Splice variants associated with neomorphic sf3b1 mutants

ABSTRACT

Splice variants associated with neomorphic SF3B1 mutations are described herein. This application also relates to methods of detecting the described splice variants, and uses for diagnosing cancer, evaluating modulators of SF3B1, and methods of treating cancer associated with mutations in SF3B1.

The present application claims the benefit of priority to U.S. Provisional Patent Application No. 62/212,876, filed Sep. 1, 2015, the contents of which are hereby incorporated by reference herein in their entirety.

The instant application contains a Sequence Listing which has been submitted electronically in ASCII format and is hereby incorporated by reference in its entirety. The ASCII copy, created on May 16, 2014, is named 12636.6-304_SL.txt and is 183 kilobytes in size.

RNA splicing, a highly regulated molecular event orchestrated by the spliceosome, results in the removal of intronic sequences from pre-mRNA to generate mature mRNA. Dysregulation of RNA splicing has been identified as a causative defect in several diseases. In addition, dysregulated splicing has been proposed to play an important role in tumorigenesis and resistance to therapy; however, the molecular causes of dysregulated splicing in cancer have remained elusive.

SF3B1 is a protein involved in RNA splicing. It forms part of the U2 snRNP complex which binds to the pre-mRNA at a region containing the branchpoint site and is involved in early recognition and stabilization of the spliceosome at the 3′ splice site (3′ ss). A thorough and systematic analysis of the effects of SF3B1 mutations is needed to define their effects on RNA splicing in cells and may lead to novel therapeutic approaches for SF3B1 mutant cancers.

The description provided herein demonstrates that certain SF3B1 mutations result in neomorphic activity with the production of known and novel splicing alterations. In addition, lineage-specific splicing aberrations were identified in chronic lymphocytic leukemia (CLL), melanoma, and breast cancer. Furthermore, treatment of SF3B1-mutant cancer cell lines, xenografts, and CLL patient samples with modulators of SF3B1 reduced aberrant splicing and induced tumor regression.

SUMMARY

The methods described herein involve detecting or quantifying the expression of one or more splice variants in a cell containing a neomorphic mutant SF3B1 protein. Various embodiments of the invention include detecting or quantifying splice variants to determine whether a patient has a cancer with one or more neomorphic SF3B1 mutations. Additional embodiments include measuring the amount of a splice variant to evaluate the effects of a compound on a mutant SF3B1 protein. Further embodiments include methods of treating a patient who has cancer cells with a neomorphic mutant SF3B1 protein.

Various embodiments encompass a method of detecting one or more splice variants selected from rows 1-790 of Table 1 in a biological sample, comprising:

a) providing a biological sample suspected of containing one or more splice variants;

b) contacting the biological sample with one or more nucleic acid probes capable of specifically hybridizing to the one or more splice variants, and

c) detecting the binding of the one or more probes to the one or more splice variants.

In some embodiments, the one or more nucleic acid probes capable of specifically hybridizing to the one or more splice variants each comprise a label. In some embodiments, the method of detecting one or more splice variants selected from rows 1-790 of Table 1 in a biological sample further comprises contacting the biological sample with one or more additional nucleic acid probes, wherein the additional probes are each labeled with a molecular barcode.

Embodiments further encompass a method of modulating the activity of a neomorphic mutant SF3B1 protein in a target cell, comprising applying an SF3B1-modulating compound to the target cell, wherein the target cell has been determined to express one or more aberrant splice variants selected from rows 1-790 of Table 1 at a level that is increased or decreased relative to the level in a cell not having the neomorphic mutant SF3B1 protein.

Embodiments also encompass a method for evaluating the ability of a compound to modulate the activity of a neomorphic mutant SF3B1 protein in a target cell, comprising the steps of:

a) providing a target cell having a mutant SF3B1 protein;

b) applying the compound to the target cell; and

c) measuring the expression level of one or more splice variants selected from row 1-790 of Table 1.

In some embodiments, the method for evaluating the ability of a compound to modulate the activity of a neomorphic mutant SF3B1 protein in a target cell further comprises the step of measuring the expression level of one or more splice variants selected from row 1-790 of Table 1 before step (b).

In some embodiments, the neomorphic mutant SF3B1 protein is selected from K700E, K666N, R625C, G742D, R625H, E622D, H662Q, K666T, K666E, K666R, G740E, Y623C, T663I, K741N, N626Y, T663P, H662R, G740V, D781E, or R625L. In some embodiments, the neomorphic mutant SF3B1 protein is selected from E622D, E622K, E622Q, E622V, Y623C, Y623H, Y623S, R625C, R625G, R625H, R625L, R625P, R625S, N626D, N626H, N626I, N626S, N626Y, H662D, H662L, H662Q, H662R, H662Y, T663I, T663P, K666E, K666M, K666N, K666Q, K666R, K666S, K666T, K700E, V701A, V701F, V701I, I704F, I704N, I704S, I704V, G740E, G740K, G740R, G740V, K741N, K741Q, K741T, G742D, D781E, D781G, or D781N.

In some embodiments, the step of measuring the expression level of one or more splice variants comprises using an assay to quantify nucleic acid selected from nucleic acid barcoding (e.g. NanoString®), RT-PCR, microarray, nucleic acid sequencing, nanoparticle probes (e.g. SmartFlare™), and in situ hybridization (e.g. RNAscope®).

In some embodiments, the step of measuring the expression level of one or more splice variants comprises measuring the number of copies of the one or more splice variant RNAs in the target cell.

In further embodiments, the compound is selected from a small molecule, an antibody, an antisense molecule, an aptamer, an RNA molecule, and a peptide. In further embodiments, the small molecule is selected from pladienolide and a pladienolide analog. In additional embodiments, the pladienolide analog is selected from pladienolide B, pladienolide D, E7107, a compound of formula 1:

a compound of formula 2:

a compound of formula 3:

or a compound of formula 4:

In some embodiments, the target cell is obtained from a patient suspected of having myelodysplastic syndrome, chronic lymphocytic leukemia, chronic myelomonocytic leukemia, or acute myeloid leukemia. In some embodiments, the target cell is obtained from a sample selected from blood or a blood fraction or is a cultured cell derived from a cell obtained from a sample chosen from blood or a blood fraction. In some embodiments, the target cell is a lymphocyte.

In further embodiments, the target cell is obtained from a solid tumor. In some embodiments, the target cell is a breast tissue cell, pancreatic cell, lung cell, or skin cell.

In some embodiments, one or more of the aberrant variants are selected from rows 1, 7, 9, 10, 13, 15, 16, 18, 21, 24, 27, 28, 30, 31, 33, 34, 48, 51, 62, 65, 66, 71, 72, 81, 84, 89, 91, 105, 107, 121, 135, 136, 152, 178, 235, 240, 247, 265, 267, 272, 276, 279, 282, 283, 286, 292, 295, 296, 298, 302, 306, 329, 330, 331, 343, 350, 355, 356, 360, 364, 372, 378, 390, 391, 423, 424, 425, 426, 431, 433, 438, 439, 443, 445, 447, 448, 451, 452, 458, 459, 460, 462, 468, 469, 472, 500, 508, 517, 519, 521, 524, 525, 527, 528, 530, 533, 536, 540, 543, 548, 545, 554, 556, 559, 571, 573, 580, 582, 583, 597, 601, 615, 617, 618, 639, 640, 654, 657, 666, 670, 680, 727, 730, 750, 758, 767, or 774 of Table 1.

In some embodiments, one or more of the aberrant variants are selected from rows 21, 31, 51, 81, 118, 279, 372, 401, 426, 443, 528, 543, 545, 548 or 566 of Table 1.

Embodiments further encompass a method for treating a patient with a neoplastic disorder, comprising administering a therapeutically effective amount of an SF3B1-modulating compound to the patient, wherein a cell from the patient has been determined to:

-   -   a) contain a neomorphic mutant SF3B1 protein; and     -   b) express one or more aberrant splice variants selected from         rows 1-790 of Table 1 at a level that is increased or decreased         relative to the level in a cell not having the neomorphic mutant         SF3B1 protein.

Additional embodiments are set forth in the description which follows.

It is to be understood that both the foregoing general description and the following detailed description are exemplary and explanatory only and are not restrictive of the invention, as claimed.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a schematic diagram depicting modes of alternative splicing.

FIG. 2 is a graph depicting levels of gene expression for abnormally spliced genes across different cancers in patient samples.

FIG. 3 is a schematic diagram showing the locations of certain neomorphic mutations in the SF3B1 protein and corresponding coding regions of the SF3B1 gene.

FIG. 4 is a graph depicting levels of aberrant splice variants detected in RNA isolated from pancreatic, lung cancer, and Nalm-6 isogenic cell lines using a NanoString® assay. Data are represented as the mean of three replicates.

FIG. 5 is a set of western blot images that confirm overexpression of SF3B1 proteins in 293FT cells.

FIG. 6 is a graph depicting levels of aberrant splice variants in RNA isolated from 293FT cells expressing wild type SF3B1 (SF3B1^(WT)) or mutant SF3B1 proteins, as measured in a NanoString® assay. Data are represented as the mean of three replicates.

FIG. 7 is a set of western blot images that confirm overexpression of SF3B1 proteins in 293FT cells.

FIG. 8 is a graph depicting levels of aberrant splice variants in RNA isolated from 293FT cells expressing SF3B1^(WT) or mutant SF3B1 proteins, as measured in a NanoString® assay.

FIG. 9A depicts a set of western blot images showing expression of SF3B1 alleles before and after shRNA-knockdown in Panc 05.04 cells. FIG. 9B depicts a graph showing levels of SF3B1 RNA detected by qPCR in Panc 05.04 cells before and after shRNA-knockdown of all SF3B1 alleles (“SF3B1^(PAN)) or SF3B1^(WT) or mutant SF3B1 (SF3B1^(MUT)) alleles. qPCR data are represented as fold change relative to pLKO non-treated with doxycycline (mean±SD, n=3). Solid black, outlined, and gray bars indicate SF3B1^(PAN), SF3B1^(WT), and SF3B1^(MUT) allele-specific qPCR data, respectively.

FIG. 10A depicts a set of western blot images showing expression of SF3B1 alleles before and after shRNA-knockdown in Panc 10.05 cells. FIG. 10B depicts a graph showing levels of SF3B1 RNA detected by qPCR in Panc 10.05 cells before and after shRNA-knockdown of SF3B1 alleles. qPCR data are represented as fold change relative to pLKO non-treated with doxycycline (mean±SD, n=3). Solid black, outlined, and gray bars indicate SF3B1^(PAN), SF3B1^(WT), and SF3B1^(MUT) allele-specific qPCR data, respectively.

FIGS. 11A and 11B are a set of graphs depicting levels of splice variants in Panc 05.04 (FIG. 11A) and Panc 10.05 cells (FIG. 11B) before and after shRNA-knockdown of SF3B1 alleles, as measured in a NanoString® assay. Data are represented as mean of three biological replicates.

FIG. 12 is a set of graphs depicting growth curves of Panc 05.04 cells before (circles) and after (squares) shRNA-knockdown of SF3B1 alleles.

FIG. 13 is a set of graphs depicting growth curves of Panc 10.05 cells before (circles) and after (squares) shRNA-knockdown of SF3B1 alleles.

FIGS. 14A and 14B are a set of images of culture plates showing colony formation of Panc 05.04 cells (FIG. 14A) and Panc 10.05 (FIG. 14B) cells before and after shRNA-knockdown of SF3B1 alleles.

FIGS. 15A and 15B are a set of graphs showing the level of splicing of pre-mRNA Ad2 substrate in nuclear extracts from (FIG. 15A) 293F cells expressing Flag-tag SF3B1^(WT) or SF3B1^(K700E) (left and right panels [circles and triangles], respectively) and (FIG. 15B) Nalm-6 (SF3B1^(WT)) and Nalm-6 SF3B1^(700E) cells (left and right panels [circles and triangles], respectively) treated with varying concentrations of E7101. Data are represented as mean±SD, n=2.

FIG. 16A depicts a pair of graphs showing the binding of a radiolabeled E7107 analog to either SF3B1^(WT) (circles, left panel) or SF3B1^(K700E) (triangles, right panel) after incubation of the proteins with varying concentrations of E7107. FIG. 16B depicts upper panels, a pair of graphs showing the levels of EIF4A1 pre-mRNA (squares) and SLC25A19 mature RNA (inverted triangles) in Nalm-6 SF3B1^(K700K) cells (left panel) and Nalm-6 SF3B1^(K700E) cells (right panel) treated with varying concentrations of E7107, as measured by qPCR. FIG. 16B depicts lower panels, a pair of graphs showing the levels of abnormally spliced isoforms of abnormally spliced genes COASY (triangles) and ZDHHC16 (diamonds) in Nalm-6 SF3B1^(K700K) cells (left panel) and Nalm-6 SF3B1^(K700E) cells (right panel) treated with varying concentrations of E7107, as measured by qPCR. qPCR data in (FIG. 16B) are represented as mean±SD (n=3).

FIG. 17 is a set of graphs depicting levels of splice variants in Nalm-6 SF3B1^(K700K) and Nalm-6 SF3B1^(K700E) cells after treatment of cells with E7107 for two or six hours, as measured in a NanoString® assay. Data are expressed as fold change from DMSO-only treatment

FIG. 18 is a set of graphs depicting levels of splice variants in Nalm-6 SF3B1^(K700K) and Nalm-6 SF3B1^(K700E) cells after treatment of cells with E7107 for six hours, as measured by RNA-Seq analysis.

FIG. 19 is a set of graphs depicting levels of splice variants in Nalm-6 SF3B1^(K700K) and Nalm-6 SF3B1^(K700E) cells after treatment of cells with the numbered compounds indicated above the graphs, as measured by RNA-Seq analysis.

FIG. 20 is set of graphs depicting levels of splice variants in Nalm-6 SF3B1^(K700K) and Nalm-6 SF3B1^(K700E) cells at varying times following treatment of cells with E7107, as measured by qPCR of RNA. Data are represented as mean±SD (n=3). The upper panels of FIG. 20 depict the levels of EIF4A1 pre-mRNA (squares) and SLC25A19 mature RNA (inverted triangles) in Nalm-6 SF3B1^(K700K) cells (left panel) and Nalm-6 SF3B1^(K700E) cells (right panel) detected at certain times after treatment with E7107. The lower panels of FIG. 20 depict the levels of abnormally spliced isoforms of abnormally spliced genes COASY (triangles) and ZDHHC16 (diamonds) in Nalm-6 SF3B1^(K700K) cells (left panel) and Nalm-6 SF3B1^(K700E) cells (right panel) detected at certain times after treatment with E7107. Open circles show the concentration of E7107 (in μg/ml [right vertical axis]) as determined by mass spectrometry of tumor samples.

FIG. 21 is a set of graphs depicting levels of canonical and aberrant splice variants in Nalm-6 SF3B1^(K700K)- and Nalm-6 SF3B1^(K700E)-xenograft tumors (left and right sets of panels, respectively) at certain timepoints after treatment of xenograft mice with E7107, as measured in a NanoString® assay. Data are represented as mean of three replicates.

FIG. 22 is a set of graphs depicting levels of canonical and aberrant splice variants in Panc 05.04-xenograft tumors at certain timepoints after treatment of xenograft mice with E7107 at various concentrations, as measured in a NanoString® assay (n=4 mice for each group).

FIG. 23 is a graph depicting tumor volume (shown as mean±SEM) in Nalm-6 SF3B1^(K700E)-xenograft mice following treatment with E7107, with control mice treated with vehicle shown by open circles (n=10 animals for each group). For E7107-treated animals, inverted triangles=1.25 mg/kg, triangles=2.5 mg/kg, and squares=5 mg/kg.

FIG. 24 is a graph depicting survival rates in 10-animal cohorts of Nalm-6 SF3B1^(K700E)-xenograft mice following treatment with E7107, with an untreated cohort shown by the solid black line. For E7107-treated animals, dashed line=1.25 mg/kg, gray line=2.5 mg/kg, and dotted line=5 mg/kg.

FIG. 25 is set of graphs depicting levels of splice variants in SF3B1^(WT) and neomorphic SF3B1 mutant CLL cell samples following treatment with 10 nM E7107 for 6 hours, as measured by analysis. Data are represented as mean values (n=3).

DESCRIPTION OF THE EMBODIMENTS

In certain aspects, the methods of the invention provide assays for measuring the amount of a splice variant in a cell, thereby determining whether a patient has a cancer with a neomorphic SF3B1 mutation. In some embodiments, at least one of the measured splice variants is an aberrant splice variant associated with a neomorphic mutation in an SF3B1 protein. In additional aspects, the measurement of a splice variant in a cell may be used to evaluate the ability of a compound to modulate a mutant neomorphic SF3B1 protein in a cell.

To assist in understanding the present invention, certain terms are first defined. Additional definitions are provided throughout the application.

As used herein, the term “mutant SF3B1 protein” includes SF3B1 proteins that differ in amino acid sequence from the human wild type SF3B1 protein set forth in SEQ ID NO:1200 (GenBank Accession Number NP_036565, Version NP_036565.2) (S. Bonnal, L. Vigevani, and J. Valcarcel, “The spliceosome as a target of novel antitumour drugs,” Nat. Rev. Drug Discov. 11:847-59 [2012]). Certain mutant SF3B1 proteins are “neomorphic” mutants, which refers to mutant SF3B1 proteins that are associated with differential expression of aberrant splice variants. In certain embodiments, neomorphic SF3B1 mutants include K700E, K666N, R625C, G742D, R625H, E622D, H662Q, K666T, K666E, K666R, G740E, Y623C, T663I, K741N, N626Y, T663P, H662R, G740V, D781E, or R625L. In other embodiments, neomophic SF3B1 mutants include E622D, E622K, E622Q, E622V, Y623C, Y623H, Y623S, R625C, R625G, R625H, R625L, R625P, R625S, N626D, N626H, N626I, N626S, N626Y, H662D, H662L, H662Q, H662R, H662Y, T663I, T663P, K666E, K666M, K666N, K666Q, K666R, K666S, K666T, K700E, V701A, V701F, V701I, I704F, I704N, I704S, I704V, G740E, G740K, G740R, G740V, K741N, K741Q, K741T, G742D, D781E, D781G, or D781N. Certain SF3B1 mutations are not associated with expression of aberrant splice variants, including K700R.

The term “splice variant” as used herein includes nucleic acid sequences that span a junction either between two exon sequences or across an intron-exon boundary in a gene, where the junction can be alternatively spliced. Alternative splicing includes alternate 3′ splice site selection (“3′ss”), alternate 5′ splice site selection (“5′ss”), differential exon inclusion, exon skipping, and intron retention (FIG. 1). Certain splice variants associated with a given genomic location may be referred to as wild type, or “canonical,” variants. These splice variants are most abundantly expressed in cells that do not contain a neomorphic SF3B1 mutant protein. Additional splice variants may be referred to as “aberrant” splice variants, which differ from the canonical splice variant and are primarily associated with the presence of a neomorphic SF3B1 mutant protein in a cell. Aberrant splice variants may alternatively be referred to as “abnormal” or “noncanonical” splice variants. In certain circumstances, cells with a wild type or non-neomorphic SF3B1 protein have low or undetected amounts of an aberrant splice variant, while cells with a neomorphic SF3B1 protein have levels of an aberrant splice variant that are elevated relative to the low or undetected levels in the wild type SF3B1 cells. In some cases, an aberrant splice variant is a splice variant that is present in a wild type SF3B1 cell but is differentially expressed in a cell that has a neomorphic SF3B1 mutant, whereby the latter cell has a level of the aberrant splice variant that is elevated or reduced relative to the level in the wild type SF3B1 cell. Different types of cells containing a neomorphic SF3B1 mutant, such as different types of cancer cells, may have differing levels of expression of certain aberrant splice variants. In addition, certain aberrant splice variants present in one type of cell containing a neomorphic SF3B1 mutant may not be present in other types of cells containing a neomorphic SF3B1 mutant. In some cases, patients with a neomorphic SF3B1 mutant protein may not express an aberrant splice variant or may express an aberrant splice variant at lower levels, due to low allelic frequency of the neomorphic SF3B1 allele. The identity and relative expression levels of aberrant splice variants associated with various types of cells containing neomorphic SF3B1 mutants, such as certain cancer cells, will be apparent from the description and examples provided herein.

The term “evaluating” includes determining the ability of a compound to treat a disease associated with a neomorphic SF3B1 mutation. In some instances, “evaluating” includes determining whether or to what degree a compound modulates aberrant splicing events associated with a neomorphic SF3B1 protein. Modulation of the activity of an SF3B1 protein may encompass up-regulation or down-regulation of aberrant splice variant expression associated with a neomorphic SF3B1 protein. Additionally, “evaluating” includes distinguishing patients that may be successfully treated with a compound that modulates the expression of splice variants associated with a neomorphic SF3B1 protein.

The use of the word “a”, “an” or “the” when used in conjunction with the term “comprising” in the claims or the specification may mean “one,” but it is also consistent with the meaning of “one or more,” “at least one,” and “one or more than one.” “Or” is to be read inclusively to mean “and/or” unless explicitly indicated to refer to alternatives only, such as where alternatives are mutually exclusive.

Splice Variants

Splice variants of the invention are listed in Table 1. Table 1 provides the genomic location of each canonical (“WT”) and aberrant (“Ab.”) splice junction, as well as the sequence. Each sequence listed in the table contains 20 nucleotides from each of the 3′ and 5′ sides of a splice junction (i.e., the splice junction is at the midpoint of the listed nucleotide sequence). The “Avg WT %” and “Avg Ab. %” columns provide the average percentage count that the canonical (WT) or aberrant splice variant, respectively, represented out of the total counts of all splice variants that utilize a shared splice site, where the counts were determined as set forth in Example 1. The “Log₂ Fold Change” column provides the log₂ of the fold change observed between percentage counts of canonical and aberrant cohorts (see Example 1). The “FDR Q-Value” column provides, as a measure of statistical significance, q-values calculated using the Benjamini-Hochberg procedure from p-values, which in turn were determined using the moderated t-test defined in the Bioconductor's limma package (available at http://www.bioconductor.org) (see Example 1). The “Event” column indicates the nature of the aberrant splice variant, where “3′ss” indicates alternate 3′ splice site selection, “5′ss” indicates alternate 5′ splice site selection, “exon incl.” indicates differential exon inclusion, and “exon skip” indicates exon skipping. The “Type” column refers to the cancer type of the sample in which the aberrant splice variant was identified, where “Br.” indicates breast cancer, “CLL” indicates chronic lymphocytic leukemia, and “Mel.” indicates melanoma.

TABLE 1 Aberrant Avg Avg Log2 Aberrant sequence (SEQ WT sequence WT Ab. Fold FDR Q- junction WT junction ID NO) (SEQ ID NO) % % Diff. Value Event Type 1 chr2: chr2: AGCAAGTAGAAG AGCAAGTAGAAG 0 56 5.83 6.30E−07 3′ss Br. 109102364-109102954 109102364-109102966 TCTATAAAATTT TCTATAAAATAC ACCCCCAGATAC AGCTGGCTGAAA AGCT (1) TAAC (2) 2 chr16: chr16: CGGGCCGCATCA CGGGCCGCATCA 0 51 5.70 2.38E−07 3′ss Br. 708344-708509 708344-708524 TCCGGGAGAGCA TCCGGGAGCTGC CTGTGTTCCAGC CCGGTGTCCACC TGCC (3) CTGA (4) 3 chr3: chr3: CTGGAGCCGGCG CTGGAGCCGGCG 0 51 5.70 2.19E−07 3′ss Br. 50380021-50380348 50380000-50380348 GGAAGGAGTGTG GGAAGGAGGCAA CTGGTTCCTCTC GCTGCAGCAGTT CCCA (5) CGAG (6) 4 chr19: chr19: GGCCCTTTTGTC GGCCCTTTTGTC 0 48 5.61 2.32E−06 3′ss Br. 57908542-57909780 57908542-57909797 CTCACTAGCATT CTCACTAGGTTC TCTGTTCTGACA TTGGCATGGAGC GGTT (7) TGAG (8) 5 chr2: chr2: TGGGAGGAGCAT TGGGAGGAGCAT 0 47 5.58 7.79E−07 3′ss Br. 97285513-97297048 97285499-97297048 GTCAACAGAGTT GTCAACAGGACT TCCCTTATAGGA GGCTGGACAATG CTGG (9) GCCC (10) 6 chr19: chr19: GATGGTGGATGA GATGGTGGATGA 0 46 5.55 1.10E−05 3′ss Br. 23545541-23556543 23545527-23556543 ACCCACAGTTTT ACCCACAGGTAT TTTTTTTCAGGT ATGTCCTCATTT ATAT (11) TCCT (12) 7 chr10: chr10: TACCTCTGGTTC TACCTCTGGTTC 0 46 5.55 3.63E−09 3′ss Br. 99214556-99215395 99214556-99215416 CTGTGCAGTCTT CTGTGCAGTTCT CGCCCCTCTTTT GTGGCACTTGCC CTTA (13) CTGG (14) 8 chr18: chr18: TTGGACCGGAAA TTGGACCGGAAA 0 44 5.49 4.30E−09 3′ss Br. 683395-685920 683380-685920 AGACTTTGAGTC AGACTTTGATGA TCTTTTTGCAGA TGGATGCCAACC TGAT (15) AGCG (16) 9 chr17: chr17: ACCCAAGCCTTG ACCCAAGCCTTG 0 44 5.49 1.50E−07 exon Br. 40714237-40714373 40714237-40714629 AGGTTTCATTTC AGGTTTCAGCCT incl. CCCCTCCCAGGA GGGCAGCATGGC TTTC (17) CGTA (18) 10 chr5: chr5: AGCATTGCTAGA AGCATTGCTAGA 0 41 5.39 4.86E−09 3′ss Br. 139815842-139818078 139815842-139818045 AGCAGCAGCTTT AGCAGCAGGAAT TGCAGATCCTGA TGGCAAATTGTC GGTA (19) AACT (20) 11 chr1: chr1: CAAGTATATGAC CAAGTATATGAC 0 39 5.32 1.31E−10 3′ss Br. 245246990-245288006 245246990-245250546 TGAAGAAGATCC TGAAGAAGGTGA TGAATTCCAGCA GCCTTTTTCTCA AAAC (21) AGAG (22) 12 chr3: chr3: TGCAGTTTGGTC TGCAGTTTGGTC 0 36 5.21 9.63E−09 3′ss Br. 9960293-9962150 9960293-9962174 AGTCTGTGCCTT AGTCTGTGGGCT CCTCACCCCTCT CTGTGGTATATG CCTC (23) ACTG (24) 13 chr1: chr1: TCTTTGGAAAAT TCTTTGGAAAAT 0 29 4.91 3.27E−07 3′ss Br. 101458310-101460665 101458296-101460665 CTAATCAATTTT CTAATCAAGGGA CTGCCTATAGGG AGGAAGATCTAT GAAG (25) GAAC (26) 14 chr7: chr7: GTATCAAAGTGT GTATCAAAGTGT 0 28 4.86 5.02E−05 3′ss Br. 94157562-94162500 94157562-94162516 GGACTGAGATTT GGACTGAGGATT GTCTTCCTTTAG CCATTGCAAAGC GATT (27) CACA (28) 15 chr20: chr20: AGAACTGCACCT AGAACTGCACCT 0 27 4.81 1.50E−07 3′ss Br. 62701988-62703210 62701988-62703222 ACACACAGCCCT ACACACAGGTGC GTTCACAGGTGC AGACCCGCAGCT AGAC (29) CTGA (30) 16 chr17: chr17: GGAGCAGTGCAG GGAGCAGTGCAG 0 25 4.70 9.63E−06 3′ss Br. 71198039-71199162 71198039-71199138 TTGTGAAATCAT TTGTGAAAGTTT TACTTCTAGATG TGATTCATGGAT ATGC (31) TCAC (32) 17 chr17: chr17: CTATTTCACTCT CTATTTCACTCT 0 25 4.70 5.99E−08 3′ss Br. 7131030-7131295 7131102-7131295 CCCCCGAACCTA CCCCCGAAATGA TCCAGGTTCCTC GCCCATCCAGCC CTCC (33) AATT (34) 18 chr20: chr20: TTTGCAGGGAAT TTTGCAGGGAAT 0 25 4.70 2.72E−07 3′ss Br. 35282126-35284762 35282104-35284762 GGGCTACATCCC GGGCTACATACC CTTGGTTCTCTG ATCTGCCAGCAT TTAC (35) GACT (36) 19 chr2: chr2: TGACCACGGAGT TGACCACGGAGT 0 25 4.70 1.61E−06 3′ss Br. 232196609-232209660 232196609-232209686 ACCTGGGGCCCT ACCTGGGGATCA TTTTTCTCTTTC TGACCAACACGG CTTC (37) GGAA (38) 20 chr17: chr17: AGACCTACCAGA AGACCTACCAGA 0 24 4.64 7.16E−06 3′ss Br. 62574712-62576906 62574694-62576906 AGGCTATGTGTT AGGCTATGAACA TATTAATTTTAC GAGGACAACGCA AGAA (39) ACAA (40) 21 chr12: chr12: ATTTGGACTCGC ATTTGGACTCGC 0 23 4.58 8.14E−08 3′ss Br. 105601825-105601935 105601807-105601935 TAGCAATGATGT TAGCAATGAGCA CTGTTTATTTTT TGACCTCTCAAT AGAG (41) GGCA (42) 22 chr12: chr12: CATGTGGAATCC CATGTGGAATCC 0 22 4.52 1.87E−04 3′ss Br. 53836517-53837270 53836517-53837174 CAATGCCGGCCC CAATGCCGGGCA CTGTCCTCCTCC GCCAGGGCCAAA CCCA (43) TCCA (44) 23 chr22: chr22: CTGGGAGGTGGC CTGGGAGGTGGC 0 22 4.52 2.76E−08 3′ss Br. 19044699-19050714 19044675-19050714 ATTCAAAGCCCC ATTCAAAGGCTC ACCTTTTGTCTC TTCAGAGGTGTT CCCA (45) CCTG (46) 24 chr11: chr11: GGATGACCGGGA GGATGACCGGGA 0 21 4.46 4.61E−08 3′ss Br. 71939542-71939690 71939542-71939770 TGCCTCAGTCAC TGCCTCAGATGG TTTACAGCTGCA GGAGGATGAGAA TCGT (47) GCCC (48) 25 chr20: chr20: ACATGAAGGTGG ACATGAAGGTGG 0 21 4.46 2.63E−08 3′ss Br. 34144042-34144725 34144042-34144743 ACGGAGAGGCTC ACGGAGAGGTAC CCCTCCCACCCC TGAGGACAAATC AGGT (49) AGTT (50) 26 chr6: chr6: AGAGAAGTCGTT AGAGAAGTCGTT 2 64 4.44 2.91E−10 3′ss Br. 31919381-31919565 31919381-31919651 TCATTCAAGTCA TCATTCAAGTTG GCTAAGACACAA GTGTAATCAGCT GCAG (51) GGGG (52) 27 chr1: chr1: TCACTCAAACAG TCACTCAAACAG 0 20 4.39 9.99E−07 3′ss Br. 179835004-179846373 179834989-179846373 TAAACGAGTTTT TAAACGAGGTAT ATCATTTACAGG GTGACGCATTCC TATG (53) CAGA (54) 28 chr1: chr1: CGATCTCCCAAA CGATCTCCCAAA 0 20 4.39 1.35E−09 3′ss Br. 52880319-52880412 52880319-52880433 AGGAGAAGTCTG AGGAGAAGCCCC ACCAGTCTTTTC TCCCCTCGCCGA TACA (55) GAAA (56) 29 chr8: chr8: TTATTTTACACA TTATTTTACACA 0 20 4.39 1.49E−09 3′ss Br. 38095145-38095624 38095145-38095606 ATCCAAAGCCAG ATCCAAAGCTTA TTGCAGGGTCTG TGGTGCATTACC ATGA (57) AGCC (58) 30 chr19: chr19: TGCCTGTGGACA TGCCTGTGGACA 0 19 4.32 2.37E−05 3′ss Br. 14031735-14034130 14031735-14034145 TCACCAAGCCTC TCACCAAGGTGC GTCCTCCCCAGG CGCCTGCCCCTG TGCC (59) TCAA (60) 31 chr14: chr14: AGTTAGAATCCA AGTTAGAATCCA 0 18 4.25 1.65E−10 3′ss Br. 74358911-74360478 74358911-74360499 AACCAGAGTGTT AACCAGAGCTCC GTCTTTTCTCCC TGGTACAGTTTG CCCA (61) TTCA (62) 32 chr19: chr19: ATATGCTGGAAT ATATGCTGGAAT 0 18 4.25 8.07E−08 3′ss Br. 45314603-45315482 45314603-45315419 GGTTCCTTGTCA GGTTCCTTACCG CAATGCACGACA ACCGCTCGGGAG CCCG (63) CTCG (64) 33 chr1: chr1: ATCAGAAATTCG ATCAGAAATTCG 0 18 4.25 4.25E−08 3′ss Br. 212515622-212519131 212515622-212519144 TACAACAGGTTT TACAACAGCTCC CTTTTAAAGCTC TGGAGCTTTTTG CTGG (65) ATAG (66) 34 chr9: chr9: AAATGAAGAAAC AAATGAAGAAAC 0 18 4.25 1.31E−10 3′ss Br. 125759640-125760854 125759640-125760875 TCCTAAAGCCTC TCCTAAAGATAA TCTCTTTCTTTG AGTCCTGTTTAT TTTA (67) GACC (68) 35 chr11: chr11: CATAAAATTCTA CATAAAATTCTA 0 17 4.17 1.35E−06 3′ss Br. 4104212-4104471 4104212-4104492 ACAGCTAATTCT ACAGCTAAGCAA CTTTCCTCTGTC GCACTGAGCGAG TTCA (69) GTGA (70) 36 chr12: chr12: GCCTGCCTTTGA GCCTGCCTTTGA 0 17 4.17 3.58E−07 3′ss Br. 113346629-113348840 113346629-113348855 TGCCCTGGATTT TGCCCTGGGTCA TGCCCGAACAGG GTTGACTGGCGG TCAG (71) CTAT (72) 37 chr17: chr17: CCAAGCTGGTGT CCAAGCTGGTGT 0 17 4.17 4.19E−04 3′ss Br. 78188582-78188831 78188564-78188831 GCGCACAGGCCT GCGCACAGGCAT CTCTTCCCGCCC CATCGGGAAGAA AGGC (73) GCAC (74) 38 chr20: chr20: CTCCTTTGGGTT CTCCTTTGGGTT 0 17 4.17 2.67E−07 3′ss Br. 45354963-45355453 45354963-45355502 TGGGCCAGGCCC TGGGCCAGTGAC CAGGTCCCACCA CTGGCTTGTCCT CAGC (75) CAGC (76) 39 chr12: chr12: AATATTGCTTTA AATATTGCTTTA 0 16 4.09 2.79E−07 3′ss Br. 116413154-116413319 116413118-116413319 CCAAACAGGGAC CCAAACAGGTCA CCCTTCCCCTTC CGGAGGAGTAAA CCCA (77) GTAT (78) 40 chr14: chr14: CAGTTATAAACT CAGTTATAAACT 0 16 4.09 4.46E−07 3′ss Br. 71059726-71060012 71059705-71060012 CTAGAGTGAGTT CTAGAGTGCTTA TATTTTCCTTTT CTGCAGTGCATG ACAA (79) GTAT (80) 41 chr16: chr16: GCCTGCCCCGGA GCCTGCCCCGGA 0 15 4.00 7.77E−06 3′ss Br. 30012851-30016688 30012851-30016541 AACTCAAGATGT AACTCAAGATGG TCAGCGATGCAG CGGTGGGACCCC GTAG (81) CCGA (82) 42 chr17: chr17: TTCAGGAGGTGG TTCAGGAGGTGG 0 15 4.00 3.26E−05 3′ss Br. 57148329-57153007 57148308-57153007 AGCACCAGATAA AGCACCAGTTGC TTTTTTTCCTCA GGTCTTGTAGTA CACA (83) AGAG (84) 43 chr16: chr16: GGATCCTTCACC GGATCCTTCACC 0 14 3.91 3.01E−07 3′ss Br. 1402307-1411686 1402307-1411743 CGTGTCTGTCTT CGTGTCTGGACC TGCAGACAGGTT CGTGCATCTCTT CTGT (85) CCGA (86) 44 chr3: chr3: ATTTGGATCCTG ATTTGGATCCTG 0 14 3.91 8.71E−07 3′ss Br. 196792335-196792578 196792319-196792578 TGTTCCTCTTTT TGTTCCTCATAC TTTCTGTTAAAG AACTAGACCAAA ATAC (87) ACGA (88) 45 chr14: chr14: AGATGTCAGGTG AGATGTCAGGTG 0 13 3.81 1.55E−05 3′ss Br. 75356052-75356580 75356052-75356599 GGAGAAAGCCTT GGAGAAAGCTGT TGATTGTCTTTT TGGAGACACAGT CAGC (89) TGCA (90) 46 chr18: chr18: AGAAAGAGCATA AGAAAGAGCATA 0 13 3.81 9.84E−07 3′ss Br. 33605641-33606862 33573263-33606862 AATTGGAAATAT AATTGGAAGAGT TGGACATGGGCG ACAAGCGCAAGC TATC (91) TAGC (92) 47 chr1: chr1: TCAGCCCTCTGA TCAGCCCTCTGA 0 13 3.81 6.10E−07 3′ss Br. 226036315-226036597 226036255-226036597 ACTACAAAGGTG ACTACAAAACAG TTTGTTCACAGA AAGAGCCTGCAA GATC (93) GTGA (94) 48 chr6: chr6: CCGGGGCCTTCG CCGGGGCCTTCG 3 51 3.70 1.35E−09 3′ss Br. 10723474-10724788 10723474-10724802 TGAGACCGCTTG TGAGACCGGTGC TTTTCTGCAGGT AGGCCTGGGGTA GCAG (95) GTCT (96) 49 chr2: chr2: CAAGTCCATCTC CAAGTCCATCTC 0 12 3.70 5.71E−03 3′ss Br. 132288400-132289210 132288400-132289236 TAATTCAGGGTC TAATTCAGGCAA TGACTTGCAGCC GGCCAGGCCCCA AACT (97) GCCC (98) 50 chr2: chr2: CAAGATAGATAT CAAGATAGATAT 0 12 3.70 4.26E−06 3′ss Br. 170669034-170671986 170669016-170671986 TATAGCAGGTGG TATAGCAGAACT CTTTTGTTTTAC TCGATATGACCT AGAA (99) GCCA (100) 51 chr15: chr15: GAAACCAACTAA GAAACCAACTAA 1 24 3.64 4.30E−09 3′ss Br. 59209219-59224554 59209198-59224554 AGGCAAAGCCCA AGGCAAAGGTAA TTTTCCTTCTTT AAAACATGAAGC CGCA (101) AGAT (102) 52 chr11: chr11: GGGGACAGTGAA GGGGACAGTGAA 0 11 3.58 5.99E−08 3′ss Br. 57100545-57100908 57100623-57100908 ATTTGGTGGCAA ATTTGGTGGGCA GAATGAGGTGAC GCTGCTTTCCTT ACTG (103) TGAC (104) 53 chr1: chr1: CTCAGAGCCAGG CTCAGAGCCAGG 0 11 3.58 3.15E−07 3′ss Br. 35871069-35873587 35871069-35873608 CTGTAGAGATGT CTGTAGAGTCCG TTTCTACCTTTC CTCTATCAAGCT CACA (105) GAAG (106) 54 chr2: chr2: GAGGAGCCACAC GAGGAGCCACAC 0 11 3.58 2.22E−07 3′ss Br. 220044485-220044888 220044485-220044831 TCTGACAGATAC TCTGACAGTGAG CTGGCTGAGAGC GGTGCGGGGTCA TGGC (107) GGCG (108) 55 chr5: chr5: ACTCGCGCCTCT ACTCGCGCCTCT 0 11 3.58 7.04E−07 3′ss Br. 150411955-150413168 150411944-150413168 TCCATCTGTTTT TCCATCTGCCGG GTCGCAGCCGGA AATACACCTGGC ATAC (109) GTCT (110) 56 chrX: chrX: ACTTCCTTAGTG ACTTCCTTAGTG 0 11 3.58 7.37E−07 3′ss Br. 47059013-47059808 47059013-47060292 GTTTCCAGGTTG GTTTCCAGGTGG CCAGGGCACTGC TGGTGCTCACCA AGCT (111) ACAC (112) 57 chrX: chrX: GTCTTGAGAATT ACTTCCTTAGTG 0 11 3.58 6.70E−06 5′ss Br. 47059943-47060292 47059013-47060292 GGAAGCAGGTGG GTTTCCAGGTGG TGGTGCTCACCA TGGTGCTCACCA ACAC (113) ACAC (112) 58 chr20: chr20: TCCAGAGCCCAC TCCAGAGCCCAC 2 34 3.54 4.87E−09 3′ss Br. 330007-330259 330007-330281 AGTCCCAGCTGC AGTCCCAGGGGT ACCTTACCTGCT CCATGATGCCGA CCCC (114) GCTG (115) 59 chr18: chr18: CCAAGTTTTGTG CCAAGTTTTGTG 1 22 3.52 1.96E−05 3′ss Br. 224200-224923 224179-224923 AAAGAAAGTGTA AAAGAAAGAACA TGTTTTGTTCAC TCAGATACCAAA GACA (116) CCTA (117) 60 chr11: chr11: TCTTCACAGAAC TCTTCACAGAAC 0 10 3.46 2.99E−08 3′ss Br. 47195466-47196565 47195391-47196565 ACACTCAAGTGC ACACTCAACCCC TTGTAGGTCTTG CTGCCTGGGATG GTGC (118) CGCC (119) 61 chr12: chr12: GAGAAGCTCACG TCTTGGAGGAGC 0 10 3.46 4.11E−02 exon Br. 56604352-56606779 56604352-56607741 ATTACCAGGCAC CAGTACAGGCAC incl. CTCATTGTGAAC CTCATTGTGAAC ATGC (120) ATGC (121) 62 chr14: chr14: GTGGGGGGCCAT GTGGGGGGCCAT 0 10 3.46 3.25E−08 3′ss Br. 23237380-23238985 23237380-23238999 TGCTGCATTTTG TGCTGCATGTAC TATTTTCCAGGT AGTCTTTGCCCG ACAG (122) CTGC (123) 63 chr17: chr17: TACTGAAATGTG TACTGAAATGTG 0 10 3.46 2.49E−05 3′ss Br. 34942628-34943454 34942628-34943426 ATGAACATATCC ATGAACATATCC AGGTAATCGAGA AGAAGCTTGGAA GACC (124) GCTG (125) 64 chr1: chr1: GAATCTCTTATC GAATCTCTTATC 0 10 3.46 2.93E−06 3′ss Br. 145581564-145583935 145581564-145583914 ATTGATGGTTCC ATTGATGGTTTA TGTTCAGATTGT TTTATGGAGATT GATG (126) CTTA (127) 65 chr5: chr5: CTCCATGCTCAG CTCCATGCTCAG 1 20 3.39 6.76E−06 3′ss Br. 869519-870587 865696-870587 CTCTCTGGTTTC CTCTCTGGGGAA TTTCAGGGCCTG GGTGAAGAAGGA CCAT (128) GCTG (129) 66 chr12: chr12: CTTGGAGCTGAC CTTGGAGCTGAC 7 79 3.32 1.30E−08 3′ss Br. 107378993-107380746 107379003-107380746 GCCGACGGGGAA GCCGACGGTTTA CTGACAAGATCA TTGCAGGGAACT CATT (130) GACA (131) 67 chr7: chr7: TCCAGCCTGGGC CTATCAAAAGAG 1 19 3.32 4.35E−08 exon Br. 8261028-8267267 8261028-8268230 GACAGAAGTCTT GATATGTTTCTT incl. GTCTCAAGAAGA GTCTCAAGAAGA AAAC (132) AAAC (133) 68 chr10: chr10: TGCGGAGCAAGA TGCGGAGCAAGA 0 9 3.32 1.37E−04 3′ss Br. 5497081-5498027 5497081-5498049 GTGGACATCGTT GTGGACATAAAC TGTTTCCCATTT TTTACATTTTCC CTCC (134) TGTT (135) 69 chr11: chr11: AGTCCAGCCCCA AGTCCAGCCCCA 0 9 3.32 4.66E−07 3′ss Br. 64900740-64900940 64900723-64900940 GCATGGCACCTC GCATGGCAGTCC TCCCCACTCCTA TGTACATCCAGG GGTC (136) CCTT (137) 70 chr19: chr19: CAAGCAGGTCCA CAAGCAGGTCCA 0 9 3.32 1.49E−09 3′ss Br. 5595521-5598803 5595508-5598803 AAGAGAGATTTT AAGAGAGAAGCT GGTAAACAGAGC CCAAGAGTCAGG TCCA (138) ATCG (139) 71 chr22: chr22: CTCTCTCCAACC CTCTCTCCAACC 0 9 3.32 8.58E−06 3′ss Br. 39064137-39066874 39064137-39066888 TGCATTCTCATC TGCATTCTTTGG TCGCCCACAGTT ATCGATCAACCC GGAT (140) GGGA (141) 72 chr9: chr9: CACCACGCCGAG CACCACGCCGAG 2 28 3.27 2.13E−08 3′ss Br. 125023777-125026993 125023787-125026993 GCCACGAGACAT GCCACGAGTATT TGATGGAAGCAG TCATAGACATTG AAAC (142) ATGG (143) 73 chr15: chr15: GCCTCACTGAGC GCCTCACTGAGC 1 18 3.25 5.94E−09 exon Br. 25207356-25212175 25207356-25213078 AACCAAGAGTAG AACCAAGAGTGT incl. TGACTTGTCAGG CAGTTGTACCCG AGGA (144) AGGC (145) 74 chr9: chr9: GGGAGATGGATA GGGAGATGGATA 3 35 3.17 6.19E−08 3′ss Br. 35813153-35813262 35813142-35813262 CCGACTTGCTCA CCGACTTGTGAT ATTTCAGTGATC CAACGATGGGAA AACG (146) GCTG (147) 75 chr6: chr6: AGGATGTGGCTG AGGATGTGGCTG 1 17 3.17 5.18E−06 3′ss Br. 31602334-31602574 31602334-31602529 GCACAGAAGTGT GCACAGAAATGA CATCAGGTCCCT GTCAGTCTGACA GCAG (148) GTGG (149) 76 chr11: chr11: TTCTCCAGGACC TTCTCCAGGACC 0 8 3.17 6.00E−04 3′ss Br. 125442465-125445146 125442465-125445158 TTGCCAGACCTT TTGCCAGAGGAA TTCTATAGGGAA TCAAAGACTCCA TCAA (150) TCTG (151) 77 chr13: chr13: AGCTGAAATTTC AGCTGAAATTTC 0 8 3.17 1.20E−06 3′ss Br. 113915073-113917776 113915073-113917800 CAGTAAAGGGGG CAGTAAAGCCTG GTTTTATTCTTC GAGATTTGAAAA TTTT (152) AGAG (153) 78 chr16: chr16: GATGTCACTGTG GATGTCACTGTG 0 8 3.17 4.76E−02 3′ss Br. 14966186-14968874 14966186-14968892 ACTATCAAGGGC ACTATCAAGTCT CGTCTTTCTTCT TCCATCGACAGT AGGT (154) GAAC (155) 79 chr2: chr2: TATCCATTCCTG TATCCATTCCTG 0 8 3.17 2.22E−07 3′ss Br. 178096758-178097119 178096736-178097119 AGTTACAGTATA AGTTACAGTGTC AACTTCCTTCTC TTAATATTGAAA ATGC (156) ATGA (157) 80 chrX: chrX: TACAAGAGCTGG TACAAGAGCTGG 0 8 3.17 2.14E−05 3′ss Br. 153699660-153699819 153699660-153699830 GTGGAGAGGGTC GTGGAGAGGTAT CCAACAGGTATT TATCGAGACATT ATCG (158) GCAA (159) 81 chr19: chr19: AGCCATTTATTT AGCCATTTATTT 3 31 3.00 7.42E−06 3′ss Br. 9728842-9730107 9728855-9730107 GTCCCGTGGGAA GTCCCGTGGGTT CCAATCTGCCCT TTTTTCCAGGGA TTTG (160) ACCA (161) 82 chr1: chr1: AGTTACAACGAA AGTTACAACGAA 2 23 3.00 8.51E−06 3′ss Br. 185056772-185060696 185056772-185060710 CACCTCAGTGAC CACCTCAGGAGG TCTTTTACAGGA CAATAACAGATG GGCA (162) GCTT (163) 83 chr15: chr15: TCACACAGGATA GCCTCACTGAGC 1 15 3.00 3.25E−08 exon Br. 25212299-25213078 25207356-25213078 ATTTGAAAGTGT AACCAAGAGTGT incl. CAGTTGTACCCG CAGTTGTACCCG AGGC (164) AGGC (145) 84 chr11: chr11: CGGCGCGGGCAA CGGCGCGGGCAA 0 7 3.00 1.28E−08 3′ss Br. 62648919-62649352 62648919-62649364 CCTGGCGGCCCC CCTGGCGGGTCT CATTTCAGGTCT GAAGGGGCGTCT GAAG (165) CGAT (166) 85 chr11: chr11: CCACCGCCATCG CCACCGCCATCG 0 7 3.00 4.87E−09 3′ss Br. 64877395-64877934 64877395-64877953 ACGTGCAGTACC ACGTGCAGGTGG TCTTTTTACCAC GGCTCCTGTACG CAGG (167) AAGA (168) 86 chr19: chr19: CTATGGGCTCAC CTATGGGCTCAC 0 7 3.00 1.24E−03 3′ss Br. 41084118-41084353 41084118-41084367 TCCTCTGGTCCT TCCTCTGGTTCG CCTGTTGCAGTT TCGCCTGCAGCT CGTC (169) TCGA (170) 87 chr1: chr1: TATCTCTGGGAA TATCTCTGGGAA 0 7 3.00 3.66E−06 3′ss Br. 35917392-35919157 35917377-35919157 AAAACACATTTC AAAACACAGGGA TTTTTTTGCAGG CCTGATGGGGTG GGAC (171) CAGC (172) 88 chr22: chr22: TCATCCAGAGCC TCATCCAGAGCC 0 7 3.00 1.95E−06 3′ss Br. 50966161-50966940 50966146-50966940 CAGAGCAGGGGA CAGAGCAGATGC TGTCTGACCAGA AAGTGCTGCTGG TGCA (173) ACCA (174) 89 chr9: chr9: CCAAGGACTGCA CCAAGGACTGCA 0 7 3.00 8.14E−08 3′ss Br. 139837449-139837800 139837395-139837800 CTGTGAAGGCCC CTGTGAAGATCT CCGCCCCGCGAC GGAGCAACGACC CTGG (175) TGAC (176) 90 chr1: chr1: CCCGAGCTCAGA CCCGAGCTCAGA 4 38 2.96 2.79E−08 3′ss Br. 3548881-3549961 3548902-3549961 GAGTAAATTCTC GAGTAAATATGA CTTACAGACACT GATCGCCTCTGT GAAA (177) CCCA (178) 91 chr19: chr19: GTGCTTGGAGCC GTGCTTGGAGCC 3 29 2.91 3.56E−07 3′ss Br. 55776746-55777253 55776757-55777253 CTGTGCAGACTT CTGTGCAGCCTG TCCGCAGGGTGT GTGACAGACTTT GCGC (179) CCGC (180) 92 chr1: chr1: GCTGGACACGCT GCTGGACACGCT 1 14 2.91 2.38E−07 exon Br. 39332671-39338689 39333282-39338689 GACCAAGGCATC GACCAAGGTGTT skip ACTTAGGAGCTG GGTAGCCTTATA CTAC (181) TGAA (182) 93 chr2: chr2: CCCCTGAGATGA CCCCTGAGATGA 1 14 2.91 1.82E−07 exon Br. 27260570-27260682 27260570-27261013 AGAAAGAGCTCC AGAAAGAGCTCC incl. CTGTTGACAGCT TGAGCAGCCTGA GCCT (183) CTGA (184) 94 chr2: chr2: CTGAACTTTGGG CTGAACTTTGGG 3 28 2.86 7.09E−06 3′ss Br. 233599948-233600472 233599948-233612324 CCTGAATGATGT CCTGAATGGCTC GTTTGGACCCCG CGAGCTCTGTCC AATA (185) AGTG (186) 95 chr11: chr11: AGATCGCCTGGC AGATCGCCTGGC 0 6 2.81 4.87E−09 3′ss Br. 3697619-3697738 3697606-3697738 TCAGTCAGTTTT TCAGTCAGACAT TCTCTCTAGACA GGCCAAACGTGT TGGC (187) AGCC (188) 96 chr11: chr11: GGAGGTGGACCT GGAGGTGGACCT 0 6 2.81 1.25E−06 3′ss Br. 68363686-68367788 68363686-68367808 GAGTGAACAATT GAGTGAACCACC TCTCCCCTCTTT CAACTGGTCAGC TTAG (189) TAAC (190) 97 chr12: chr12: TACAGATGGTAA TACAGATGGTAA 0 6 2.81 8.19E−07 3′ss Br. 72315234-72316743 72315234-72316762 AATGCAAGTTTG AATGCAAGGAAT ATTTTTCATATC TGCCACAAGCAG CAGG (191) TCTG (192) 98 chr16: chr16: CCCTGCTCATCA CCCTGCTCATCA 0 6 2.81 5.11E−07 3′ss Br. 685022-685280 684956-685280 CCTACGGGTCTG CCTACGGGCCCT TCCCAGGCTCTC ATGCCATCAATG TGGG (193) GGAA (194) 99 chr1: chr1: GGCTCCCATTCT GGCTCCCATTCT 0 6 2.81 3.43E−04 3′ss Br. 155630724-155631097 155630704-155631097 GGTTAAAGAGTG GGTTAAAGGCCA TTCTCATTTCCA GTCTGCCATCCA ATAG (195) TCCA (196) 100 chr1: chr1: CTGCACTTATAA CTGCACTTATAA 0 6 2.81 1.50E−06 3′ss Br. 47108988-47110832 47108973-47110832 ATATTCAGTGTT ATATTCAGACCC CCACCTTGCAGA GAGGGGAAGCTG CCCG (197) CAGC (198) 101 chr22: chr22: CGCTGGCACCAT CGCTGGCACCAT 0 6 2.81 1.29E−02 3′ss Br. 36627480-36629198 36627512-36629198 GAACCCAGTATT GAACCCAGAGAG TCCAGGACCAAG CAGTATCTTTAT TGAG (199) TGAG (200) 102 chr6: chr6: CCCTAGTCTGAT AGAGAAGTCGTT 0 6 2.81 6.01E−04 5′ss Br. 31919565-31919651 31919381-31919651 TCCTTTAGGTTG TCATTCAAGTTG GTGTAATCAGCT GTGTAATCAGCT GGGG (201) GGGG (52) 103 chr1: chr1: TTCCCCATCAAC TTCCCCATCAAC 3 26 2.75 6.26E−07 3′ss Br. 19480448-19481411 19480433-19481411 ATCAAAAGTTTT ATCAAAAGTTCC GTTGTCTGCAGT AATGGTGGCAGT TCCA (202) AAGA (203) 104 chr11: chr11: CCAGCTGCATTG CCAGCTGCATTG 4 32 2.72 6.93E−04 3′ss Br. 67161081-67161193 67161081-67161161 CAAGTTCGGACT CAAGTTCGGGGT GTGAGTCCCTGC GCGGAAGACTCA AGGC (204) CAAC (205) 105 chr12: chr12: GGCCAGCCCCCT GGCCAGCCCCCT 6 41 2.58 1.26E−09 3′ss Br. 120934019-120934204 120934019-120934218 TCTCCACGGCCT TCTCCACGGTAA TGCCCACTAGGT CCATGTGCGACC AACC (206) GAAA (207) 106 chr14: chr14: CGCTCTCCGCCT AGGGAGACGTTC 2 17 2.58 1.96E−05 exon Br. 75348719-75352288 75349327-75352288 TCCAGAAGGGGT CCTGCCTGGGGT skip CTCCTTATGCCA CTCCTTATGCCA GGGA (208) GGGA (209) 107 chr1: chr1: TTGGAAGCGAAT TTGGAAGCGAAT 1 11 2.58 1.14E−07 3′ss Br. 23398690-23399766 23398690-23399784 CCCCCAAGTCCT CCCCCAAGTGAT TTGTTCTTTTGC GTATATCTCTCA AGTG (210) TCAA (211) 108 chr11: chr11: CTACGGCGGTGC CTACGGCGGTGC 0 5 2.58 1.09E−07 3′ss Br. 44957237-44958353 44957213-44958353 CCTCCTCACCCC CCTCCTCAGCAT CTTTTCATCCCC CTCCCTGATCAT CGCC (212) GTGG (213) 109 chr12: chr12: CCTGGTCGCAGT CCTGGTCGCAGT 0 5 2.58 9.89E−04 exon Br. 57494682-57496072 57493873-57496072 TCAACAAGATGA TCAACAAGGAGA incl. GGAATCTGATGC TCCTGCTGGGCC TCAG (214) GTGG (215) 110 chr16: chr16: CACCAAGCAGAG CACCAAGCAGAG 0 5 2.58 1.04E−07 3′ss Br. 15129410-15129852 15129410-15129872 GCTTCCAGTCTG GCTTCCAGGCCA TCTGCCCTTTCT GAAGCCTTTTAA GTAG (216) AAGG (217) 111 chr17: chr17: GGGACTCCCCCA GGGACTCCCCCA 0 5 2.58 9.75E−05 3′ss Br. 41164294-41164946 41164294-41165063 AAGACAAGCTTT AAGACAAGGTCC TCTTTCAGTAAA CATTTTCAGTGC TGTA (218) CCAA (219) 112 chr17: chr17: GCACTGCTGTTC GCACTGCTGTTC 0 5 2.58 1.25E−05 3′ss Br. 61511981-61512446 61511955-61512446 AACCTCGGCTTC AACCTCGGGGGC TCCCTTCCTCTC AAGTATAGCGCA ACCC (220) TTTG (221) 113 chr19: chr19: ACGAGACCATTG ACGAGACCATTG 0 5 2.58 1.71E−05 3′ss Br. 2247021-2247564 2247021-2247592 CCTTCAAGGAGC CCTTCAAGGTGC CCTCTCTGTCCC CGAGCAGAGAGA CCGC (222) TCGA (223) 114 chr21: chr21: AAGATGTCCCTG AAGATGTCCCTG 0 5 2.58 5.11E−07 3′ss Br. 38570326-38572514 38570326-38572532 TGAGGATTGTGT TGAGGATTGCAC GTTTGTTTCCAC TGGGTGCAAGTT AGGC (224) CCTG (225) 115 chr6: chr6: AGAGAAGTCGTT AGAGAAGTCGTT 0 5 2.58 2.67E−07 3′ss Br. 31919381-31919551 31919381-31919651 TCATTCAATCTG TCATTCAAGTTG ATTCCTTTAGGT GTGTAATCAGCT CAGC (226) GGGG (52) 116 chrX: chrX: AGCCCAGCAGTT AGCCCAGCAGTT 0 5 2.58 5.15E−07 3′ss Br. 48751114-48751182 48751100-48751182 CCGAAATGTCTC CCGAAATGCGCC CCTTCTCCAGCG CCCATTCCTGGA CCCC (227) GGAC (228) 117 chr17: chr17: CCCTCCCCCGGC ACCCAAGCCTTG 2 16 2.50 3.35E−04 exon Br. 40714505-40714629 40714237-40714629 TCCTGTCGGCCT AGGTTTCAGCCT incl. GGGCAGCATGGC GGGCAGCATGGC CGTA (229) CGTA (18) 118 chr15: chr15: TGATTCCAAGCA TGATTCCAAGCA 1 10 2.46 1.54E−06 3′ss Br. 25213229-25219533 25213229-25219457 AAAACCAGCCTT AAAACCAGGCTC CCCCTAGGTCTT CATCTACTCTTT CAGA (230) GAAG (231) 119 chr2: chr2: CAAGTCCATCTC CAAGTCCATCTC 2 15 2.42 6.24E−03 3′ss Br. 132288400-132289224 132288400-132289236 TAATTCAGCCAA TAATTCAGGCAA CTCTCAAGGCAA GGCCAGGCCCCA GGCC (232) GCCC (98) 120 chr7: chr7: CTATCAAAAGAG CTATCAAAAGAG 2 15 2.42 9.00E−05 exon Br. 8267481-8268230 8261028-8268230 GATATGTTCATT GATATGTTTCTT incl. TTAGGAGGCCAA GTCTCAAGAAGA GGCA (233) AAAC (133) 121 chr3: chr3: GTCTTCCAATGG GTCTTCCAATGG 7 41 2.39 2.38E−07 3′ss Br. 148759467-148759952 148759455-148759952 CCCCTCAGCCTT CCCCTCAGGAAA TTCTCTAGGAAA TGATACACCTGA TGAT (234) AGAA (235) 122 chr8: chr8: GCACCTCCCCGG GCACCTCCCCGG 4 25 2.38 3.96E−02 exon Br. 144873910-144874045 144873610-144874045 GACGCCTGCCCT GACGCCTGTCAC incl. TGTCTGGAAAGA CGGACTTTGCTG AGTT (236) AGGA (237) 123 chr17: chr17: TGGACCCCAGAC GTCCCGGAACCA 1 9 2.32 5.71E−03 exon Br. 3828735-3831533 3828735-3831956 CACACCGGAAGA CATGCACGAAGA incl. AATGAGCCAGAA AATGAGCCAGAA GTGA (238) GTGA (239) 124 chr11: chr11: TCTGTGTTCCCA TGTATGACGTCA 0 4 2.32 2.08E−03 5′ss Br. 66040546-66043274 66039931-66043274 TCGCACAGGAAT CTGACCAGGAAT CCTACGCCAACG CCTACGCCAACG TGAA (240) TGAA (241) 125 chr12: chr12: GGAATATGATCC GGAATATGATCC 0 4 2.32 6.10E−04 3′ss Br. 15272132-15273996 15264351-15273996 CACCCTCGTACT CACCCTCGAATC TCTCAAAGAGGA AACCTACCGACA TGGC (242) CCAA (243) 126 chr16: chr16: GAACTGGCACCG GAACTGGCACCG 0 4 2.32 1.02E−06 3′ss Br. 313774-313996 313774-314014 ACAGACAGTGTC ACAGACAGATCC CCCTCCCTCCCC TGTTTCTGGACC AGAT (244) TTGG (245) 127 chr19: chr19: TGATGAAGACCT TGATGAAGACCT 0 4 2.32 1.48E−03 3′ss Br. 44116292-44118380 44112259-44118380 TTCCCCAGATCT TTCCCCAGGCCC CTTAGGTGAAGA CGAGCATTCCTC CATG (246) TGAT (247) 128 chr1: chr1: CCAGGCCGACAT CCAGGCCGACAT 0 4 2.32 4.27E−07 3′ss Br. 228335400-228336058 228335400-228336071 GGAGAGCAGCCC GGAGAGCAGCAA CACCCACAGGCA GGAGCCCGGCCT AGGA (248) GTTT (249) 129 chr20: chr20: ACATGAAGGTGG ACATGAAGGTGG 0 4 2.32 5.15E−07 3′ss Br. 34144042-34144761 34144042-34144743 ACGGAGAGTTCT ACGGAGAGGTAC CTGTGACCAGAC TGAGGACAAATC ATGA (250) AGTT (50) 130 chr2: chr2: TTCGTCCATATG TTCGTCCATATG 0 4 2.32 2.38E−03 3′ss Br. 198267783-198268308 198267759-198268308 TGCATAAGCTTC TGCATAAGATCC TTCTCTTTTCTC TCGTGGTCATTG TTTT (251) AACC (252) 131 chr3: chr3: AGGGATGGCCAG AGAAGGGAGCGA 0 4 2.32 8.01E−04 5′ss Br. 47969840-47981988 47969840-48019354 TGGTAGTGGGTC TACTACAGGGTC TCCAACTGAATT TCCAACTGAATT CCTT (253) CCTT (254) 132 chr4: chr4: CCAATGTGGTTC CCAATGTGGTTC 0 4 2.32 1.00E−05 3′ss Br. 38907482-38910197 38907482-38910212 AAAACACATTAT AAAACACAGGTA CTCATCTGCAGG AAAGTGTCTTAA GTAA (255) CTGG (256) 133 chr7: chr7: CCATTGATGCAA CCATTGATGCAA 0 4 2.32 7.45E−03 exon Br. 94227316-94228086 94218044-94228086 ACGCAGCAATGG ACGCAGCAGAAC incl. AGTTTCGCTCCT TTGCCACATCAG GTTG (257) ACTC (258) 134 chr8: chr8: GCTGCATCTGGA CAGTGTTAGTGA 0 4 2.32 6.84E−03 5′ss Br. 17873340-17882869 17872349-17882869 GGTCCTGGGAAG ATGACTATGAAG CAGAATCTGGTA CAGAATCTGGTA ATAT (259) ATAT (260) 135 chr17: chr17: ACAAGGACACAG ACAAGGACACAG 10 53 2.30 5.76E−06 3′ss Br. 73518592-73519333 73518292-73519333 AAAACAAGCCTT AAAACAAGCTGG CCCACACAGGCC AGCACCGCTGCA CTGC (261) CCTC (262) 136 chr16: chr16: AGCTCGGACCAA AGCTCGGACCAA 9 48 2.29 1.29E−03 3′ss Br. 47495337-47497792 47495337-47497809 GCGCTCAGTTTT GCGCTCAGCTTA AAAATTGCTATA GCCTGCGACGCT GCTT (263) TATG (264) 137 chr6: chr6: AGGGGGCTCTTT AGGGGGCTCTTT 6 32 2.24 3.39E−03 3′ss Br. 91269953-91271340 91269933-91271340 ATATAATGTTTG ATATAATGTGCT TGCCTTTCTTTC GCATGGTGCTGA GCAG (265) ACCA (266) 138 chr15: chr15: GCCCCCAACTGA GCCCCCAACTGA 2 13 2.22 4.76E−03 exon Br. 41130464-41130740 41128480-41130740 GAAGCTGGGCTG GAAGCTGGTGCC incl. GAGTGCTGTGGC CTTGGTGTGGTG ACAA (267) GAAG (268) 139 chr17: chr17: GAACGAGATCTC AGTATCAGAAGG 4 21 2.14 6.40E−03 5′ss Br. 2276080-2276246 2275782-2276246 ATCCCACTAACT ACAAAAAGAACT ACAAAGAGCTGG ACAAAGAGCTGG AGCT (269) AGCT (270) 140 chr17: chr17: TGAAGGTCCAGG TGAAGGTCCAGG 8 35 2.00 4.45E−02 3′ss Br. 4885470-4886051 4885455-4886051 GCATGGAGCCTG GCATGGAGTGTC TCTCCTGGCAGT TCTATGGCTGCT GTCT (271) ACGT (272) 141 chr16: chr16: GGCGGCCGCGCC GGCGGCCGCGCC 2 11 2.00 3.29E−02 exon Br. 1728357-1733509 1728357-1735439 GGCTCCAGGAAA GGCTCCAGGGCC incl. TGGCAACTGCTG ATGAAGCCCCCA ACAG (273) GGAG (274) 142 chr11: chr11: CCTTCCAGCTAC CCTTCCAGCTAC 1 7 2.00 1.25E−04 3′ss Br. 2993509-2997253 2993473-2997253 ATCGAAACGCAT ATCGAAACTTTA GAGGATGTTGTA CCTAAAGCAGTA TTTC (275) AAAA (276) 143 chr10: chr10: CTTTTCTCTTCT GATGTGATGAAC 0 3 2.00 2.72E−03 5′ss Br. 69583150-69595149 69583150-69597691 TTTTATAGGTTG TATCTTCGGTTG AACAAATCCTGG AACAAATCCTGG CAGA (277) CAGA (278) 144 chr11: chr11: GCACTGGGCATT GCACTGGGCATT 0 3 2.00 1.28E−07 3′ss Br. 66053068-66053171 66053007-66053171 CAGAAAAGTCTC CAGAAAAGGTTC TCTTCCTCACCC TCCCCGGAGGTG CTGC (279) CTGG (280) 145 chr11: chr11: CTGTCACAGGGG CTGTCACAGGGG 0 3 2.00 2.18E−03 3′ss Br. 77090454-77090938 77090433-77090938 AGTTTACGTCTT AGTTTACGGGAA GCATGTCTCTCT TGCCAGAGCAGT TACA (281) GGGC (282) 146 chr12: chr12: GGGTGCAAAAGA GGGTGCAAAAGA 0 3 2.00 2.66E−07 3′ss Br. 57032980-57033763 57033091-57033763 TCCTGCAGCCAT TCCTGCAGGACT TCCAGGTTGCTG ACAAATCCCTCC AGGT (283) AGGA (284) 147 chr12: chr12: GGCACCCCAAAA GGCACCCCAAAA 0 3 2.00 9.82E−07 3′ss Br. 58109976-58110164 58109976-58110194 GATGGCAGATCA GATGGCAGGTGC GTCTCTCCCTGT GAGCCCGACCAA TCTC (285) GGAT (286) 148 chr17: chr17: GCATCTCAGCCC GCATCTCAGCCC 0 3 2.00 2.72E−07 3′ss Br. 16344444-16344670 16344444-16344681 AAGAGAAGTTTC AAGAGAAGGTTA TTTGCAGGTTAT TATTCCCAGAGG ATTC (287) ATGT (288) 149 chr1: chr1: CTTGCCTTCCCA CTTGCCTTCCCA 0 3 2.00 2.32E−04 3′ss Br. 154246074-154246225 154246074-154246249 TCCTCCTGCAAA TCCTCCTGAACT CACCTGCCACCT TCCAGGTCCTGA TTCT (289) GTCA (290) 150 chr1: chr1: CTACACAGAGCT CTACACAGAGCT 0 3 2.00 8.14E−08 3′ss Br. 32096333-32098095 32096443-32098095 GCAGCAAGGTGT GCAGCAAGCTCT GCACCCAGCTGC GTCCCAAATGGG AGGT (291) CTAC (292) 151 chr2: chr2: ACCTGTTACCAC ACCTGTTACCAC 0 3 2.00 1.17E−04 3′ss Br. 101622533-101635459 101622533-101622811 TTTCAAAATTTC TTTCAAAAATCT TGTGCTAAACAG ACAGACAGTCAA TGTT (293) TGTG (294) 152 chr2: chr2: AGACAAGGGATT AGACAAGGGATT 0 3 2.00 3.82E−06 3′ss Br. 26437445-26437921 26437430-26437921 GGTGGAAACATT GGTGGAAAAATT TTATTTTACAGA GACAGCGTATGC ATTG (295) CATG (296) 153 chr3: chr3: CAACGAGAACAA CAACGAGAACAA 0 3 2.00 2.29E−07 3′ss Br. 101401353-101401614 101401336-101401614 GCTATCAGTTAC GCTATCAGGGCT TTTTACCCCACA GCTAAGGAAGCA GGGC (297) AAAA (298) 154 chr5: chr5: TCTATATCCCCT TCTATATCCCCT 0 3 2.00 1.27E−06 3′ss Br. 177576859-177577888 177576839-177577888 CTAAGACGCACT CTAAGACGGACC TCTTTCCCCTCT TGGGTGCAGCCG GTAG (299) CAGG (300) 155 chr6: chr6: TGGAGCCAGTTA TGGAGCCAGTTA 0 3 2.00 9.28E−04 3′ss Br. 31506716-31506923 31506632-31506923 CTGGGCAGGTGT CTGGGCAGGTGT GTTTTTGTGACA CTGTACTGGTGA GTCA (301) TGTG (302) 156 chrX: chrX: AAAAGAAACTGA AAAAGAAACTGA 13 54 1.97 1.08E−05 3′ss Br. 129771378-129790554 129771384-129790554 GGAATCAGTATC GGAATCAGCCTT ACAGGCAGAAGC AGTATCACAGGC TCTG (303) AGAA (304) 157 chrX: chrX: CAGCACTAGGTT CAGCACTAGGTT 7 30 1.95 8.04E−04 exon Br. 135758876-135761693 135760115-135761693 ATAAAGAGGAGT ATAAAGAGAGGA skip CTAGTAAAAGCC TGTCTTATATCT CTAA (305) TAAA (306) 158 chr6: chr6: GCCCCCGTTTTC GCCCCCGTTTTC 4 18 1.93 9.28E−05 3′ss Br. 31936315-31936399 31936315-31936462 CTGCCCAGCCCT CTGCCCAGTACC TGTCCTCAGTGC TGAAGCTGCGGG ACCC (307) AGCG (308) 159 chr2: chr2: GCCGCCGCCGCC CACCTTATGAAG 10 40 1.90 4.22E−03 5′ss Br. 97757449-97760437 97757449-97757599 GCCGCCAGGCTC TATAGCAGGCTC TGATGCTGGTGT TGATGCTGGTGT CTGG (309) CTGG (310) 160 chr19: chr19: AGTGGCAGTGGC AGTGGCAGTGGC 6 25 1.89 2.97E−03 3′ss Br. 6731065-6731209 6731122-6731209 TGTACCAGCCCA TGTACCAGCTCT CAGGAAACAACC TGGTGGAGGGCT CGTA (311) CCAC (312) 161 chr16: chr16: GAGATTCTGAAG GAGATTCTGAAG 4 16 1.77 5.02E−05 3′ss Br. 54954250-54957496 54954322-54957496 ATAAGGAGTTCT ATAAGGAGGTAA CTTGTAGGATGC AACCTGTTTAGA CACT (313) AATT (314) 162 chr2: chr2: CCAAGAGACAGC CCCCTGAGATGA 4 16 1.77 3.39E−06 exon Br. 27260760-27261013 27260570-27261013 ACATTCAGCTCC AGAAAGAGCTCC incl. TGAGCAGCCTGA TGAGCAGCCTGA CTGA (315) CTGA (184) 163 chr10: chr10: TCAGAGCAGTCG CTACGACAGTGA 10 35 1.71 1.55E−02 5′ss Br. 75290593-75294357 75290593-75296026 GGACACAGGACA AGATTCAGGACA CCTGACTGATAG CCTGACTGATAG TGAA (316) TGAA (317) 164 chr1: chr1: CTGTTGTGTCCG CTGTTGTGTCCG 19 63 1.68 5.06E−05 3′ss Br. 155278867-155279833 155278867-155279854 TTTTGAAGAGCC TTTTGAAGAATG CTTTGCTCCTCC AACGGAGACCAG CTCA (318) AATT (319) 165 chr16: chr16: CCGGCCCTACAG CCCTCCGCCTCC 6 21 1.65 3.26E−02 exon Br. 630972-632882 632309-632882 GCTGGCGGATAA TGATGCAGATAA skip ACCCACTGCCCT ACCCACTGCCCT ACAG (320) ACAG (321) 166 chr16: chr16: GAGATTCTGAAG GAGATTCTGAAG 18 57 1.61 6.30E−07 3′ss Br. 54954239-54957496 54954322-54957496 ATAAGGAGGATG ATAAGGAGGTAA CCACTGGAAATG AACCTGTTTAGA TTGA (322) AATT (314) 167 chr14: chr14: TGAAAAGTCCAG TCCTGGAGGAGC 15 47 1.58 1.41E−02 5′ss Br. 39734625-39746137 39736726-39746137 AGGAAGAGGTTG TACGCAGGGTTG TGGCAGCACTGC TGGCAGCACTGC CTGA (323) CTGA (324) 168 chr13: chr13: GTCATGGCAGAA CTATAGCTACTG 10 32 1.58 1.25E−02 exon Br. 21157158-21165105 21164006-21165105 GACCTCCATCCA GATATGGGTCCA skip AGACATCTCTGG AGACATCTCTGG CATC (325) CATC (326) 169 chr17: chr17: CCGGAGCCCCTT CCGGAGCCCCTT 5 17 1.58 4.45E−02 3′ss Br. 45229302-45232037 45229284-45232037 CAAAAAAGACTT CAAAAAAGTCTG TTCGTGTTTTAC TTGCCAGAATCG AGTC (327) GCCA (328) 170 chr16: chr16: CCACAGATACTA CCACAGATACTA 3 11 1.58 1.99E−02 3′ss Br. 47484364-47485306 47462809-47485306 TTAGGAGGCCAT TTAGGAGGGAAT ACCACCCTGAAC TTATCATGGCAT GCGC (329) CCAG (330) 171 chr12: chr12: TGTTCAAGTTCC CCTGGTCGCAGT 1 5 1.58 1.50E−04 exon Br. 57493873-57494628 57493873-57496072 CAAAGCAGGAGA TCAACAAGGAGA incl. TCCTGCTGGGCC TCCTGCTGGGCC GTGG (331) GTGG (215) 172 chr16: chr16: ACTCCCAGCTCA ACTCCCAGCTCA 0 2 1.58 6.10E−05 3′ss Br. 56403209-56419830 56403239-56419830 ATGCAATGGTTC ATGCAATGGCTC CATACCATCTGG ATCAGATTCAAG TACT (332) AGAT (333) 173 chr17: chr17: ATCACTGTGACT ATCACTGTGACT 0 2 1.58 4.98E−05 3′ss Br. 80013701-80013861 80013701-80013876 TCCCTGAGGTCT TCCCTGAGCTGC CTGCTCCTCAGC TGTCCCCCAGCA TGCT (334) ACGT (335) 174 chr18: chr18: ATCCTCTCAATC ATCCTCTCAATC 0 2 1.58 4.76E−02 3′ss Br. 51729496-51731367 51715381-51731367 AAAATAAGTTTG AAAATAAGGGTA TGTGCACTTTTC AACCAGACTTGA TGCT (336) ATAC (337) 175 chr1: chr1: CTATTCCTTTAT CTATTCCTTTAT 0 2 1.58 5.34E−04 3′ss Br. 145109684-145112354 145109684-145112372 TGAATTTGTTTT TGAATTTGATAC CTTCATCATTCT TTTCATTCAGAA AGAT (338) AACC (339) 176 chr2: chr2: AGTCATACCTGG AGTCATACCTGG 0 2 1.58 3.46E−03 3′ss Br. 242274627-242275373 242274627-242275389 AGCAGCAGTTTG AGCAGCAGAAAA TTTCTTTTCTAG AATTGAAAGAAC AAAA (340) TGTC (341) 177 chr3: chr3: GCAACCAGTTTG GCAACCAGTTTG 0 2 1.58 1.37E−04 3′ss Br. 49395199-49395459 49395180-49395459 GGCATCAGCTGC GGCATCAGGAGA CCTTCTCTCCTG ACGCCAAGAACG TAGG (342) AAGA (343) 178 chr4: chr4: CCATGGTCAAAA CCATGGTCAAAA 0 2 1.58 3.60E−05 3′ss Br. 152022314-152024139 152022314-152024022 AATGGCAGCACC AATGGCAGACAA AACAGGTCCGCC TGATTGAAGCTC AAAT (344) ACGT (345) 179 chr5: chr5: GCCTGATGCCCG GCCTGATGCCCG 0 2 1.58 1.29E−02 exon Br. 1323984-1325865 1324928-1325865 AATTTCAGGCCA AATTTCAGTTTG skip TGAAGTACTTGT GCACTTACAGCG CATA (346) AATC (347) 180 chr5: chr5: AGATTGAAGCTA AGATTGAAGCTA 0 2 1.58 6.18E−06 3′ss Br. 132439718-132439902 132439718-132439924 AAATTAAGTTTT AAATTAAGGAGC CTGTCTTACCCA TGACAAGTACTT TTCC (348) GTAG (349) 181 chr5: chr5: AGCACAAGCTAT AGCACAAGCTAT 0 2 1.58 5.76E−06 3′ss Br. 44813384-44814996 44813384-44815014 GTATCAAGCATA GTATCAAGGATT ACTTTCTTCTAC CTGGAGTGAAGC AGGA (350) AGAT (351) 182 chr6: chr6: AGATGTAAAAGT AGATGTAAAAGT 0 2 1.58 5.43E−04 3′ss Br. 52546712-52548863 52546712-52548875 GTCACTGTTTTG GTCACTGTTTAC GTTTTCAGTTAC AGCTTTCTTCCT AGCT (352) GGCT (353) 183 chr7: chr7: CTGCAGCCTCCG CCATTGATGCAA 0 2 1.58 8.78E−03 exon Br. 94218044-94227241 94218044-94228086 CCTCCCAGGAAC ACGCAGCAGAAC incl. TTGCCACATCAG TTGCCACATCAG ACTC (354) ACTC (258) 184 chr15: chr15: AGGATGATGCAG AGGATGATGCAG 10 28 1.40 1.70E−03 3′ss Br. 59373483-59376300 59373483-59376327 CATCCAACTGGT CATCCAACGCGG CTTTTTGTGTTC GCACATGAACGC TGTG (355) CCCC (356) 185 chr1: chr1: TGGTGAAATGGA TGGTGAAATGGA 12 33 1.39 1.25E−03 3′ss Br. 153925126-153925280 153925111-153925280 CCCCAAAGTCTT CCCCAAAGTACC TCTCTTTCAAGT TGCTATTGAGGA ACCT (357) GAAC (358) 186 chr1: chr1: AGCTTAAAGAAC GATCAAGGCAAC 9 25 1.38 3.31E−02 exon Br. 151739775-151742647 151740709-151742647 TGTATTCGTTTG CGGGAAAGTTTG skip ACTGCAACCCTG ACTGCAACCCTG GAGT (359) GAGT (360) 187 chr19: chr19: AACACACCAACT AACACACCAACT 1 4 1.32 8.52E−04 3′ss Br. 47342877-47349249 47342835-47349249 TTGTGGAGGTCC TTGTGGAGTTCC TGGCAATCTCCG GGAACTTTAAGA TTGC (361) TCAT (362) 188 chr15: chr15: GCGGGTCTGCAG GTTCCAGGTCCT 5 13 1.22 5.55E−04 exon Br. 75631685-75632305 75632219-75632305 CCTACGCAAACT CCTGGCAGAACT skip GAAGCAGGCCCA GAAGCAGGCCCA GACC (363) GACC (364) 189 chr1: chr1: CCCGCTGCCCCA ATTCTGATATAG 5 13 1.22 1.52E−02 exon Br. 212459633-212506838 212502673-212506838 GCTCAAAGATCA TAAAAATGATCA skip GTGCTAACATCT GTGCTAACATCT TCCG (365) TCCG (366) 190 chr22: chr22: ATGAGTTTCCCA ATGAGTTTCCCA 2 6 1.22 1.59E−03 3′ss Br. 30976673-30976998 30976688-30976998 CCGATGGGGAGG CCGATGGGGAGA AAGACCGCAGGA TGTCAGCGCAGG AGGA (367) AGGA (368) 191 chr7: chr7: AGTTTATTTAAC AGTTTATTTAAC 2 6 1.22 3.40E−02 exon Br. 80535232-80545994 80458061-80545994 ATTTGATGAGCC ATTTGATGAACT incl. TACCTTGTACAA TCGAGAAACCAA TGCT (369) GACC (370) 192 chr8: chr8: CCACCTAGCAGC CCACCTAGCAGC 2 6 1.22 1.17E−03 intron Br. 145153766-145153768 145153691-145153768 CACCAGAGACCA CACCAGAGGTTA reten- GAGGTGGCACAG CAAGGGGAGAGT tion GCAG (371) GGCC (372) 193 chr9: chr9: TCCAGGATCCTG GGCAGCGGAGGG 2 6 1.22 8.61E−03 exon Br. 96285645-96289436 96278551-96289436 AGGCATGGCCAT GCGACAAACCAT incl. ATCAGCGGGAAC ATCAGCGGGAAC AAGA (373) AAGA (374) 194 chr2: chr2: GGCAACTTCGTT GGCAACTTCGTT 20 47 1.19 5.26E−03 3′ss Br. 106781255-106782511 106781240-106782511 AATATGAGCTTT AATATGAGGTCT CTACTCAACAGG ATCCAGGAAAAT TCTA (375) GGTG (376) 195 chr19: chr19: GGAGCCTGGGCA GGAGCCTGGGCA 6 15 1.19 1.98E−02 3′ss Br. 7976215-7976299 7976215-7976320 TCTCGTTGCCCT TCTCGTTGGTGG GCCCGTCTCCCT AGCTGGCAACAG CCCA (377) GACA (378) 196 chr11: chr11: CTGGTGTGCTTG CTGGTGTGCTTG 3 8 1.17 4.87E−02 exon Br. 9161795-9163486 9161401-9163486 GGAGCCAGGGTT GGAGCCAGAGAT incl. ATCATGAAGATT CACCTCCTACAC AAAT (379) CACT (380) 197 chr1: chr1: ATTGGAGGAGCT ATTGGAGGAGCT 10 23 1.13 3.12E−03 exon Br. 160252899-160254844 160253429-160254844 TCTGGAAAGATG TCTGGAAAGTGC skip CCCTCTTCGCTT TCTTGATGATTT CCCA (381) CGAT (382) 198 chr19: chr19: AATGACGTGCTG AATGACGTGCTG 7 16 1.09 1.69E−02 3′ss Br. 16641724-16643408 16641691-16643408 CACCACTGGGCC CACCACTGCCAG CTGACGCGCGGA CGCAAGCAGGCC AAGT (383) CGGG (384) 199 chr3: chr3: GCCTGGGGTGGA GCCTGGGGTGGA 9 20 1.07 3.01E−02 exon Br. 39141945-39142237 39141994-39142237 GAGGGCAGCCCC GAGGGCAGTCTG skip CCAGCTACCACA GGATGTGGCATT AGAA (385) GGCT (386) 200 chr2: chr2: GGAAATGGGACA GGAAATGGGACA 11 24 1.06 3.05E−03 3′ss Br. 230657846-230659894 230657861-230659894 GGAGGCAGAGGA GGAGGCAGCTTT TCACAGGCTTTA TCTCTCAACAGA AAAT (387) GGAT (388) 201 chr10: chr10: AGACCGACTGCC AGACCGACTGCC 5 11 1.00 2.09E−02 exon Br. 123718925-123719872 123719110-123719872 AGTAATAGGAGA AGTAATAGAGCC skip TTGTGAAGACCT TGTTAGTATTAA TTGA (389) TGAA (390) 202 chr1: chr1: TCATGCTAGCCG TCATGCTAGCCG 5 11 1.00 3.31E−02 exon Br. 44064584-44067741 44064584-44069086 AGGCCCAGTGGC AGGCCCAGGAAA incl. GGCCAGAGGAGT CCACTATCAGCG CCGA (391) GCCT (392) 203 chr1: chr1: GAAGGCAGCTGA GAAGGCAGCTGA 4 9 1.00 1.37E−03 3′ss Br. 11131045-11132143 11131030-11132143 GCAAACAGTTCT GCAAACAGCTGC CTCCCTTGCAGC CCGGGAACAGGC TGCC (393) AAAG (394) 204 chr6: chr6: GCCAACAGCCAA GCCAACAGCCAA 3 7 1.00 6.32E−03 exon Br. 109690220-109697276 109691670-109697276 TTCTACAGGTAC TTCTACAGCTAA skip AACAAATAACAC ACCCACAGTTCA TGTG (395) GCCC (396) 205 chr17: chr17: CCCATCAACTGC CCCATCAACTGC 2 5 1.00 4.46E−02 exon Br. 37873733-37879571 37873733-37876039 ACCCACTCCCCT ACCCACTCCTGT skip CTGACGTCCATC GTGGACCTGGAT ATCT (397) GACA (398) 206 chr17: chr17: GCGGAAAGAATT GCGGAAAGAATT 2 5 1.00 4.49E−02 3′ss Br. 5250220-5253766 5250220-5253745 GCATGAAGAGCG GCATGAAGTTTG ACAACAACACAA CCATCTCTTGGA CCAG (399) GCAA (400) 207 chr1: chr1: TGTGGGAATTAC AAGAAGGGATGG 2 5 1.00 7.58E−03 exon Br. 27260910-27267947 27250657-27267947 AATTCAAGCTTA CAGAGAAGCTTA incl. TCACACAGACTT TCACACAGACTT TCAG (401) TCAG (402) 208 chr5: chr5: CTTCCTCAAGTC CTTCCTCAAGTC 1 3 1.00 1.35E−02 3′ss Br. 176759270-176761284 176759247-176761284 GCCCAAAGCTCC GCCCAAAGACAA CCCGTTTCTTCT CGTGGACGACCC CCCC (403) CACG (404) 209 chr7: chr7: TCTTCGCTGGTG TCTTCGCTGGTG 1 3 1.00 8.43E−03 exon Br. 44619227-44621047 44620838-44621047 GCAAACTGTATC GCAAACTGCGGG skip GTGAAGAGCGCT TGCATCTCGACA TCCG (405) TCCA (406) 210 chr1: chr1: GCAAGAAGTACA GCAAGAAGTACA 0 1 1.00 9.69E−03 3′ss Br. 165619201-165620230 165619201-165620250 AAGTGGAGTATG AAGTGGAGTATC TGCTTTGTTGTG CTATCATGTACA ACAG (407) GCAC (408) 211 chr3: chr3: TGTAGGAGCAAT TGTAGGAGCAAT 0 1 1.00 2.54E−04 3′ss Br. 42826828-42827519 42826812-42827519 GACTGTTGCATT GACTGTTGGTAT CTTTTTCTTTAG GGGCTATTCCAT GTAT (409) GTAT (410) 212 chr8: chr8: CCTTCCTGGATC AAGTGCAGATAG 0 1 1.00 5.33E−04 exon Br. 117738411-117746515 117738411-117767904 CCCCTAAGGTGG ATGGCCTTGTGG incl. TATTAAAGATAA TATTAAAGATAA TCAA (411) TCAA (412) 213 chrX: chrX: CAGGTCTAACTC CAGGTCTAACTC 0 1 1.00 1.53E−02 3′ss Br. 54835809-54836550 54835809-54836154 GCTTCCAGGCCC GCTTCCAGGCTG CAGCAGATGAAC AAGCTTCAGAAA CTGA (413) AGGA (414) 214 chr16: chr16: CCTCCCCATACC GCCTGCCCCGGA 10 20 0.93 3.40E−02 exon Br. 30012361-30016541 30012851-30016541 TGAGCTCGATGG AACTCAAGATGG skip CGGTGGGACCCC CGGTGGGACCCC CCGA (415) CCGA (82) 215 chr6: chr6: GCAAAAGGATAT GCAAAAGGATAT 10 20 0.93 2.78E−02 3′ss Br. 43006222-43006303 43006210-43006303 ACCAGGAGCATT ACCAGGAGGGGT TATTTCAGGGGT CCTCAAGATTCG CCTC (416) AGAT (417) 216 chr6: chr6: CACTCCAATTTA CACTCCAATTTA 9 18 0.93 1.40E−02 exon Br. 135517140-135518098 135517140-135520045 TAGATTCTGATT TAGATTCTTTCT incl. CTTCATCATGGT TAAACACTTCCA GTGA (418) GTAA (419) 217 chr7: chr7: TGAGAGTCTTCA TGAGAGTCTTCA 45 85 0.90 3.07E−04 3′ss Br. 99943591-99947339 99943591-99947421 GTTACTAGTTTG GTTACTAGAGGC TCTTTCCTAGAT GGATTTCCCTGA CCAG (420) CTGA (421) 218 chr12: chr12: TTAACAGCATTT CCCAGTCATTCA 10 19 0.86 1.21E−02 intron Br. 111085013-111085015 111082934-111085015 TGTTTTGCGATT ACAGGAAGGATT reten- CCTGCCAGCTCC CCTGCCAGCTCC tion CAGG (422) CAGG (423) 219 chr4: chr4: GATGAATGCTGA GATGAATGCTGA 4 8 0.85 2.40E−02 exon Br. 141300346-141302115 141300346-141300722 CATGGATGATCT CATGGATGCAGT skip CTCTGCAAGAGT TGATGCTGAAAA AGAT (424) TCAA (425) 220 chr10: chr10: GTCAATGCTTCC GTCAATGCTTCC 18 33 0.84 3.71E−02 3′ss Br. 114905856-114910741 114905856-114910756 ATGTCCAGCTTT ATGTCCAGGTTC CTGTCTTCTAGG CCTCCCCATATG TTCC (426) GTCC (427) 221 chr16: chr16: TATGGCAAGGAG TATGGCAAGGAG 7 13 0.81 2.25E−02 3′ss Br. 30767593-30767675 30767593-30767687 GTCGACCTTCTC GTCGACCTCTGG TTTCCCAGCTGG GCCTGTGGGGTG GCCT (428) ATCT (429) 222 chr3: chr3: TGGTTTTACCTC TGGTTTTACCTC 7 13 0.81 5.98E−03 3′ss Br. 128890351-128890476 128890381-128890476 GGATAGAGACAT GGATAGAGGTTT TTGTTATCGCTG CCAGTTTGTTTC TGGT (430) CTCG (431) 223 chr1: chr1: GAATCCGTATCT GAATCCGTATCT 34 60 0.80 2.74E−04 3′ss Br. 155278756-155279833 155278756-155279854 GGGAACAGAGCC GGGAACAGAATG CTTTGCTCCTCC AACGGAGACCAG CTCA (432) AATT (433) 224 chr20: chr20: TCCAGGAGTTCC TTTGACTAGGGT 22 39 0.80 1.59E−02 exon Br. 264722-270899 264722-270199 AGGTTCCGTGTT CCAACCAGTGTT skip TCACTTCAAGCC TCACTTCAAGCC CACT (434) CACT (435) 225 chr1: chr1: GGGCCTGATGAA GGGCCTGATGAA 30 52 0.77 2.84E−03 exon Br. 53370762-53373539 53372283-53373539 TGACATCGCTTC TGACATCGCAGC skip CTCGGCAGTCAT CTTCCCTGCACC GGGA (436) CACC (437) 226 chr4: chr4: AGCCCCAGGATG AGCCCCAGGATG 16 28 0.77 1.45E−02 exon Br. 5815889-5825343 5815889-5819937 CCTCGCAGCTCT CCTCGCAGACGT skip CGGAAGAACTGG GCCTTCTGCCAT TTGT (438) GATT (439) 227 chr20: chr20: ACTTGCCTGTGA ACTTGCCTGTGA 15 26 0.75 1.83E−03 3′ss Br. 47741142-47752369 47741124-47752369 ATTTCGAGTCTT ATTTCGAGGTGG TCCCTCTGAAAC CCCGGGAGAGTG AGGT (440) GCCC (441) 228 chrX: chrX: TACCCGGGACAA TACCCGGGACAA 2 4 0.74 4.57E−02 3′ss Br. 48933637-48934088 48933604-48934088 CCCCAAGGCCGC CCCCAAGGGGCT CCACCCCACCCC CTGTGACCTCTG CCAT (442) CCCC (443) 229 chr1: chr1: CATAGTGGAAGT CATAGTGGAAGT 39 64 0.70 4.20E−07 3′ss Br. 67890660-67890765 67890642-67890765 GATAGATCTTCT GATAGATCTGGC TTTTCACATTAC CTGAAGCACGAG AGTG (444) GACA (445) 230 chr1: chr1: GCTGTACCTTCA GCTGTACCTTCA 18 29 0.66 2.84E−03 3′ss Br. 156705701-156706410 156705701-156706423 GGAACAGGCCCT GGAACAGGGTTT TTCTCCCAGGTT CCATGCTGAGCT TCCA (446) CCTG (447) 231 chr10: chr10: TAAAGCGACTCA TAAAGCGACTCA 29 46 0.65 1.78E−02 exon Br. 101507147-101514285 101507147-101510125 TTGAGCAGGAGG TTGAGCAGGCAA skip TGGTATAACAGA AAGGCAGGATTG CAGA (448) TGGT (449) 232 chr12: chr12: TGGGAATCTGGC TGGGAATCTGGC 31 49 0.64 3.09E−04 3′ss Br. 117595889-117603289 117595868-117603289 CAGAGAAGTCTT CAGAGAAGGTGC TCTGTCTTGTTT TTGACATCCTCC TGAA (450) AGCA (451) 233 chr2: chr2: AGAAAACATCGA AGAAAACATCGA 8 13 0.64 2.66E−02 exon Br. 114472772-114476730 114475427-114476730 ATTCAGAGCTTG ATTCAGAGAGTT skip ATAATGGAACTA CCAGAAGACAGC TACA (452) GAAC (453) 234 chr11: chr11: CGTCCGCCAGTC AGCCGGGCGTTG 34 53 0.63 1.78E−02 5′ss Br. 504996-507112 504996-506608 GTCCCGAGGCAT GGGGAAAGGCAT GAAGAACTCTTG GAAGAACTCTTG ACTG (454) ACTG (455) 235 chrX: chrX: ACTAATCTTCAG CAAACACCTCTT 14 22 0.62 2.22E−04 exon Br. 123224814-123227867 123224614-123227867 CATGCCATTCGG GATTATAATCGG incl. CGTGGCACAAGC CGTGGCACAAGC CTAA (456) CTAA (457) 236 chr9: chr9: CACCACAAAATC CACCACAAAATC 37 57 0.61 6.00E−04 3′ss Br. 140622981-140637822 140622981-140637843 ACAGACAGCTTG ACAGACAGCAGC CTTGCCTTTTGT TGCAGTATCTCG TTTA (458) GAAG (459) 237 chr2: chr2: CTCCTACTACAC AGAGCTCAAAGA 34 52 0.60 2.66E−02 exon Br. 152324660-152325154 152325065-152325154 AATCTAAGATTT AGTGTTTAATTT skip CAGAAATGGCCA CAGAAATGGCCA AAGA (460) AAGA (461) 238 chr12: chr12: ATTTCCAGAGGA ATTTCCAGAGGA 49 74 0.58 1.10E−04 3′ss Br. 95660408-95663814 95660408-95663826 TTTACACTTTTG TTTACACTGGTC CTTGACAGGGTC AGTGCTGCTTGC AGTG (462) CCAT (463) 239 chr7: chr7: GAGTCGGCGCCG CACAGAGAGCTG 5 8 0.58 4.45E−02 exon Br. 44880611-44887567 44880611-44882875 AGAACATGTTTC GGCTACAGTTTC skip CTGTGGGCCGCA CTGTGGGCCGCA TCCA (464) TCCA (465) 240 chr10: chr10: TGACGTTCTCTG TGACGTTCTCTG 46 68 0.55 4.09E−04 3′ss Br. 75554088-75554298 75554088-75554313 TGCTCCAGTGGT TGCTCCAGGTTC TTCTCCCACAGG CCGGCCCCCAAG TTCC (466) TCGC (467) 241 chrX: chrX: CAAACACCTCTT CAAACACCTCTT 14 21 0.55 2.21E−02 exon Br. 123224614-123224703 123224614-123227867 GATTATAACACG GATTATAATCGG incl. CAGGTAACATGG CGTGGCACAAGC ATGT (468) CTAA (457) 242 chr2: chr2: TACTCCAGCTTC TACTCCAGCTTC 30 44 0.54 8.18E−03 3′ss Br. 86398468-86400772 86398435-86400772 AGCAACAGCACC AGCAACAGCAGG TACAGAAGCGGC TGATACCCTGTC TCAA (469) GGTC (470) 243 chr17: chr17: TCTCAGCTGACG GGCATGCAACCA 13 19 0.51 4.21E−03 exon Br. 47882807-47888837 47886570-47888837 AATGCAAGGCAC GGCACCAGGCAC skip CAACGGAGAGAC CAACGGAGAGAC AGCT (471) AGCT (472) 244 chr1: chr1: TCAAATCATTTA TCAAATCATTTA 9 13 0.49 3.77E−02 3′ss Br. 109743522-109745534 109743522-109745565 CCTCCAAGCAGC CCTCCAAGAGGA CAGCTCCTGTCA CTCCTGATGGAT CCAT (473) TTGA (474) 245 chr11: chr11: AGCAAAAAGGGG AGCAAAAAGGGG 35 49 0.47 2.40E−02 3′ss Br. 502249-504823 502181-504823 TGTCTCAGAATC TGTCTCAGGCCA TCCGGCCTGTGA CTCTTCACCTCC AACT (475) ACCA (476) 246 chr6: chr6: TGTTGCCTCCGC TGGTCATGGCCA 44 60 0.44 5.91E−04 exon Br. 31611971-31612083 31611971-31612301 GGCCGCAGGACA AACCCTGGGACA incl. GCAGGTGCCAGG GCAGGTGCCAGG CTTC (477) CTTC (478) 247 chr20: chr20: TGCCTAAGGCGG TGCCTAAGGCGG 63 84 0.41 4.16E−05 3′ss Br. 30310151-30310420 30310133-30310420 ATTTGAATCTCT ATTTGAATAATC TTCTCTCCCTTC TTATCTTGGCTT AGAA (479) TGGA (480) 248 chr6: chr6: TGGTCATGGCCA TGGTCATGGCCA 51 68 0.41 4.27E−03 exon Br. 31612191-31612301 31611971-31612301 AACCCTGGGCTC AACCCTGGGACA incl. CACCCTCATCCA GCAGGTGCCAGG GCTG (481) CTTC (478) 249 chr10: chr10: TGCAGATTCCAA CCTTCCACCCAA 49 63 0.36 4.56E−02 exon Br. 34649187-34661425 34649187-34663801 AAGAAACGAAAG GGGAACTGAAAG incl. CAGAAGATGAGG CAGAAGATGAGG ATAT (482) ATAT (483) 250 chr4: chr4: AGGAGGGCCCCC AGGAGGGCCCCC 43 54 0.32 1.35E−02 3′ss Br. 860289-860743 860322-860743 TGCCGCTGGCAA TGCCGCTGCTGA CAACTCCCAGCC CCCCTTTGGCCC CTGC (484) GCTT (485) 251 chr8: chr8: AACAACTGCCCA AACAACTGCCCA 3 4 0.32 4.44E−02 3′ss Br. 99054946-99057170 99055003-99057170 GCTTTGAGTGGC GCTTTGAGGAAA AATAATATTGAA TCTGAAATAGAG CTGG (486) TACT (487) 252 chr8: chr8: GTTGTGCCCATG GTTGTGCCCATG 66 81 0.29 4.37E−02 exon Br. 48694815-48694938 48691654-48694938 ACCTCCAGGTTA ACCTCCAGTGAT incl. GGATTAATTGAG CCCAGGGCACCG TGGC (488) CCGT (489) 253 chr20: chr20: GTTAATGGGTTT GTTAATGGGTTT 57 68 0.25 2.24E−02 exon Br. 57470739-57473995 57470739-57478585 AATGGAGAGGGC AATGGAGATGAG incl. GGCGAAGAGGAC AAGGCAACCAAA CCGC (490) GTGC (491) 254 chr20: chr20: GCAAGGAGCAAC GTTAATGGGTTT 59 69 0.22 4.34E−03 exon Br. 57474040-57478585 57470739-57478585 AGCGATGGTGAG AATGGAGATGAG incl. AAGGCAACCAAA AAGGCAACCAAA GTGC (492) GTGC (491) 255 chr19: chr19: AGTTTGAGATGA AGTTTGAGATGA 79 91 0.20 2.28E−02 exon Br. 17339118-17339611 17339118-17339817 AGCGAATGGATC AGCGAATGCTCC incl. CTGGCTTCCTGG CCCTACCAGGGG ACAA (493) TCGC (494) 256 chrX: chrX: AGAAACCTTGAA AGAAACCTTGAA 84 95 0.18 4.29E−02 exon Br. 2209644-2326785 2310515-2326785 CGACAAAGTGGA CGACAAAGAGAC skip ATTTTTATACTG GTGAGTCTTGCT TGAC (495) GTGT (496) 257 chrY: chrY: AGAAACCTTGAA AGAAACCTTGAA 84 95 0.18 4.29E−02 exon Br. 2159644-2276785 2260515-2276785 CGACAAAGTGGA CGACAAAGAGAC skip ATTTTTATACTG GTGAGTCTTGCT TGAC (495) GTGT (496) 258 chr11: chr11: ACCCCTTTGGCA ACCCCTTTGGCA 0 60 5.93 5.12E−05 3′ss CLL 67815439-67815553 67815439-67816345 TCGATCCTGCCC TCGATCCTATTT TTTCCTCAGCAC GGAGCCTGGCTG AAGA (497) CCAA (498) 259 chr2: chr2: TGGGAGGAGCAT TGGGAGGAGCAT 0 59 5.91 7.08E−07 3′ss CLL 97285513-97297048 97285499-97297048 GTCAACAGAGTT GTCAACAGGACT TCCCTTATAGGA GGCTGGACAATG CTGG (9) GCCC (10) 260 chr10: chr10: TAAAGTGTTGGC TAAAGTGTTGGC 0 51 5.70 5.10E−07 3′ss CLL 93244412-93244921 93244412-93244936 TTTACTTAAATT TTTACTTAATAC TATCTTTACAGA TGCAAACAATTT TACT (499) AGTT (500) 261 chr21: chr21: ACCTCGTCAGAA ACCTCGTCAGAA 0 48 5.61 2.38E−05 3′ss CLL 47970657-47971529 47970657-47971546 ACAACCAGAGTT ACAACCAGAGGT CCCCCGTTTCTA TGGACCAGCCTC GAGG (501) AATG (502) 262 chr22: chr22: TCATCCAGAGCC TCATCCAGAGCC 0 48 5.61 3.58E−03 3′ss CLL 50966161-50966940 50966146-50966940 CAGAGCAGGGGA CAGAGCAGATGC TGTCTGACCAGA AAGTGCTGCTGG TGCA (173) ACCA (174) 263 chr13: chr13: AAAGATTTCAGA AAAGATTTCAGA 0 39 5.32 1.50E−02 3′ss CLL 26970491-26971275 26970491-26971289 AGAAATACTATT AGAAATACGTAT TCTCTTTCAGGT ACCAACTGCAGC ATAC (503) CTTA (504) 264 chr5: chr5: CCAAAAGAGGGG CTCCATGCTCAG 0 39 5.32 4.28E−05 exon CLL 865696-869359 865696-870587 ATAATGAGGGAA CTCTCTGGGGAA incl. GGTGAAGAAGGA GGTGAAGAAGGA GCTG (505) GCTG (129) 265 chr22: chr22: CTCTCTCCAACC CTCTCTCCAACC 0 38 5.29 4.92E−04 3′ss CLL 39064137-39066874 39064137-39066888 TGCATTCTCATC TGCATTCTTTGG TCGCCCACAGTT ATCGATCAACCC GGAT (140) GGGA (141) 266 chr10: chr10: TCATCTTGAAAA TCATCTTGAAAA 0 34 5.13 3.62E−05 3′ss CLL 89519557-89527429 89516679-89527429 ATGAAAATTCCT ATGAAAATGTGG ATTTTACAGCTG ATAGGCATGTAG AGGA (506) ACCT (507) 267 chr20: chr20: TTTGCAGGGAAT TTTGCAGGGAAT 0 34 5.13 3.01E−05 3′ss CLL 35282126-35284762 35282104-35284762 GGGCTACATCCC GGGCTACATACC CTTGGTTCTCTG ATCTGCCAGCAT TTAC (35) GACT (36) 268 chr10: chr10: ACCCTGTCTACC ACCCTGTCTACC 1 64 5.02 4.28E−05 3′ss CLL 102276734-102286155 102276717-102286155 AGCCTGTGTTTT AGCCTGTGGATA CTGCCACCTACA GACCATGAAGCT GGAT (508) GAAG (509) 269 chr14: chr14: AGATGTCAGGTG AGATGTCAGGTG 1 62 4.98 8.04E−09 3′ss CLL 75356052-75356580 75356052-75356599 GGAGAAAGCCTT GGAGAAAGCTGT TGATTGTCTTTT TGGAGACACAGT CAGC (89) TGCA (90) 270 chr19: chr19: TGACACAGCCCT TGACACAGCCCT 1 59 4.91 4.19E−04 3′ss CLL 16264018-16265147 16264018-16265208 GCAGGCAGGGTC GCAGGCAGAAGG CGTGCAGGACCT ATCCCGCAAACG TTCC (510) TGGA (511) 271 chr7: chr7: GCGGGGCGAGGG GCGGGGCGAGGG 1 59 4.91 8.04E−09 3′ss CLL 102074108-102076648 102074108-102076671 CAGCTCCGCGTT CAGCTCCGGGAA TCTCTGAATTCT GGAACGTCCCAG CCCC (512) GGAT (513) 272 chr1: chr1: TCTTTGGAAAAT TCTTTGGAAAAT 0 29 4.91 3.49E−03 3′ss CLL 101458310-101460665 101458296-101460665 CTAATCAATTTT CTAATCAAGGGA CTGCCTATAGGG AGGAAGATCTAT GAAG (25) GAAC (26) 273 chr7: chr7: CCACCTCACCAT CCACCTCACCAT 0 29 4.91 1.26E−02 3′ss CLL 99954506-99955849 99954506-99955842 CACCCAGGGCAG CACCCAGGCCCT CCCCTCCACAGG CAGGCAGCCCCT GCCC (514) CCAC (515) 274 chr19: chr19: GATGGTGGATGA GATGGTGGATGA 1 57 4.86 7.10E−04 3′ss CLL 23545541-23556543 23545527-23556543 ACCCACAGTTTT ACCCACAGGTAT TTTTTTTCAGGT ATGTCCTCATTT ATAT (11) TCCT (12) 275 chr3: chr3: GCCAACCTAGAG GCCAACCTAGAG 1 56 4.83 2.18E−05 3′ss CLL 108403188-108405274 108403188-108405291 CCCCCCTGCTCT CCCCCCTGATGA CTGCCTCTTACA CTGGCATAGCCT GATG (516) GGGC (517) 276 chr17: chr17: GGAGCAGTGCAG GGAGCAGTGCAG 0 27 4.81 1.14E−04 3′ss CLL 71198039-71199162 71198039-71199138 TTGTGAAATCAT TTGTGAAAGTTT TACTTCTAGATG TGATTCATGGAT ATGC (31) TCAC (32) 277 chr6: chr6: AACCGGGGGAGC AACCGGGGGAGC 0 27 4.81 8.95E−03 3′ss CLL 41040823-41046743 41040823-41046767 GAGGCACGTTTC GAGGCACGGAGT TTTCCCCACCTT GTACCTCACAGC TCTA (518) CTTC (519) 278 chr11: chr11: CACACAGACTGC CACACAGACTGC 1 54 4.78 3.38E−06 3′ss CLL 62376298-62376433 62376277-62376433 GTTCGATGAGTG GTTCGATGCCTT TCTTCCCCCTGC GCTGTTCACCCT CTTA (520) GATG (521) 279 chr14: chr14: AGTTAGAATCCA AGTTAGAATCCA 0 26 4.75 9.14E−07 3′ss CLL 74358911-74360478 74358911-74360499 AACCAGAGTGTT AACCAGAGCTCC GTCTTTTCTCCC TGGTACAGTTTG CCCA (61) TTCA (62) 280 chr11: chr11: CATAAAATTCTA CATAAAATTCTA 2 79 4.74 1.89E−06 3′ss CLL 4104212-4104471 4104212-4104492 ACAGCTAATTCT ACAGCTAAGCAA CTTTCCTCTGTC GCACTGAGCGAG TTCA (69) GTGA (70) 281 chr17: chr17: AGACCTACCAGA AGACCTACCAGA 0 25 4.70 1.18E−02 3′ss CLL 62574712-62576906 62574694-62576906 AGGCTATGTGTT AGGCTATGAACA TATTAATTTTAC GAGGACAACGCA AGAA (39) ACAA (40) 282 chr7: chr7: GTTTTTACCTCT GTTTTTACCTCT 1 49 4.64 1.80E−08 3′ss CLL 76943820-76950041 76943806-76950041 GCCTCCTGATCT GCCTCCTGGTTT CTCATCCTAGGT TCATACTCTGCA TTTC (522) CACC (523) 283 chr20: chr20: AGAACTGCACCT AGAACTGCACCT 0 24 4.64 3.30E−05 3′ss CLL 62701988-62703210 62701988-62703222 ACACACAGCCCT ACACACAGGTGC GTTCACAGGTGC AGACCCGCAGCT AGAC (29) CTGA (30) 284 chr3: chr3: CACTGCTGGGAG CACTGCTGGGAG 0 24 4.64 1.42E−07 3′ss CLL 129284872-129285369 129284860-129285369 AGTGGAAGTTGC AGTGGAAGATTC TTCCACAGATTC CTGAGAGCTGCC CTGA (524) GGCC (525) 285 chr11: chr11: GATTTTGGAGAG GATTTTGGAGAG 0 23 4.58 1.27E−04 3′ss CLL 33080641-33083060 33080641-33083075 GCAACCAACTTT GCAACCAAATTC GTTTTTCACAGA CCTGGACTTTGT TTCC (526) CACC (527) 286 chr1: chr1: TCACTCAAACAG TCACTCAAACAG 0 23 4.58 1.48E−03 3′ss CLL 179835004-179846373 179834989-179846373 TAAACGAGTTTT TAAACGAGGTAT ATCATTTACAGG GTGACGCATTCC TATG (53) CAGA (54) 287 chr2: chr2: TGCAGAACTGGA TGCAGAACTGGA 0 23 4.58 2.35E−02 3′ss CLL 23977668-23980287 23977644-23980287 TAAAGAAGTGTA TAAAGAAGGTGC TTTTTTTGTCTC TTCTAAAGTAAA AATT (528) GAAA (529) 288 chr5: chr5: ACTCTTATGCAG ACTCTTATGCAG 0 23 4.58 4.37E−03 3′ss CLL 1579622-1585098 1581810-1585098 TCCCCATGAGGT TCCCCATGAGGA TATGCTTATGTT GATCCTAGTCTC TCTC (530) ACCA (531) 289 chr6: chr6: AGTGTTTTACCA AGTGTTTTACCA 0 23 4.58 2.41E−04 3′ss CLL 30884736-30884871 30884736-30884881 TGGATGTTGTCA TGGATGTTGGCT TTCCAGGGCTCC CCTCAGTGGCTG TCAG (532) TGAC (533) 290 chr6: chr6: TTTATGATGCTG TTTATGATGCTG 0 23 4.58 1.66E−02 3′ss CLL 49416664-49419178 49416640-49419178 CTTTAAAGTTTT CTTTAAAGCTCA GTTAATGTTTTT TTAATGAAATTG CTTT (534) AAGA (535) 291 chr8: chr8: ATCTAAAAACAG ATCTAAAAACAG 0 23 4.58 3.15E−03 3′ss CLL 61741365-61742868 61741365-61742880 AAGAGCAGGTCC AAGAGCAGGTGC TTTTTTAGGTGC AAAAACTTCAAG AAAA (536) CTAT (537) 292 chr2: chr2: AGCAAGTAGAAG AGCAAGTAGAAG 2 68 4.52 3.76E−08 3′ss CLL 109102364-109102954 109102364-109102966 TCTATAAAATTT TCTATAAAATAC ACCCCCAGATAC AGCTGGCTGAAA AGCT (1) TAAC (2) 293 chr15: chr15: GGATTGCAGCCA GGATTGCAGCCA 0 22 4.52 5.30E−05 3′ss CLL 72859518-72862504 72859518-72862517 ACACAAAGTTTC ACACAAAGGAAT TCTTCATAGGAA GTCCCAAATGCC TGTC (538) ATGT (539) 294 chr5: chr5: GGTTTCGAGTTT GGTTTCGAGTTT 0 22 4.52 1.57E−02 3′ss CLL 109181707-109183328 109181707-109183357 GAATAGTGTTTT GAATAGTGGTCA GCTTGTTTGTTT GATTGAAGTTAT GTTT (540) CATG (541) 295 chr9: chr9: AAATGAAGAAAC AAATGAAGAAAC 0 22 4.52 5.36E−04 3′ss CLL 125759640-125760854 125759640-125760875 TCCTAAAGCCTC TCCTAAAGATAA TCTCTTTCTTTG AGTCCTGTTTAT TTTA (67) GACC (68) 296 chr11: chr11: GGATGACCGGGA GGATGACCGGGA 2 65 4.46 7.66E−06 3′ss CLL 71939542-71939690 71939542-71939770 TGCCTCAGTCAC TGCCTCAGATGG TTTACAGCTGCA GGAGGATGAGAA TCGT (47) GCCC (48) 297 chr11: chr11: CCACCGCCATCG CCACCGCCATCG 2 65 4.46 2.31E−08 3′ss CLL 64877395-64877934 64877395-64877953 ACGTGCAGTACC ACGTGCAGGTGG TCTTTTTACCAC GGCTCCTGTACG CAGG (167) AAGA (168) 298 chr19: chr19: TGCCTGTGGACA TGCCTGTGGACA 0 21 4.46 1.50E−04 3′ss CLL 14031735-14034130 14031735-14034145 TCACCAAGCCTC TCACCAAGGTGC GTCCTCCCCAGG CGCCTGCCCCTG TGCC (59) TCAA (60) 299 chr11: chr11: CGCAAGTACTTC CGCAAGTACTTC 0 20 4.39 2.24E−03 3′ss CLL 64676597-64676742 64676622-64676742 CTGCCCCATCCA CTGCCCCAGGTA GCAGCACACAGT GTGGTGACTGTG GGGA (542) AACC (543) 300 chr22: chr22: TTCATAACAAAC TCATCAATGCCC 0 20 4.39 1.08E−04 5′ss CLL 24210086-24210667 24204389-24210667 CAGTAAATCACA CGACCTTGCACA TTCAGGAATTCA TTCAGGAATTCA CCAA (544) CCAA (545) 301 chr2: chr2: AAATTTAACATT AAATTTAACATT 0 20 4.39 2.96E−02 3′ss CLL 24207701-24222524 24207701-24222541 ACTCATAGTTTT ACTCATAGAGTA TGCTGTTTTACA AGCCATATCAAA GAGT (546) GACT (547) 302 chr11: chr11: CACCGGGAGCTG CACCGGGAGCTG 2 59 4.32 8.17E−07 3′ss CLL 64119858-64120198 64119858-64120215 CAGGGCCGCCCC CAGGGCCGGCAC TTGTCCATCCCA GAGCAGCTGCAG GGCA (548) GCCC (549) 303 chr11: chr11: GGAGGTGGACCT GGAGGTGGACCT 0 19 4.32 5.52E−04 3′ss CLL 68363686-68367788 68363686-68367808 GAGTGAACAATT GAGTGAACCACC TCTCCCCTCTTT CAACTGGTCAGC TTAG (189) TAAC (190) 304 chr11: chr11: ATTGGACACAGA CTGTCTCTAGGC 0 19 4.32 5.03E−04 5′ss CLL 984190-984644 981299-984644 GATGGGATATCG TAAGCAGAATCG TGACGTCTGCAT TGACGTCTGCAT CCAC (550) CCAC (551) 305 chr17: chr17: GGGACCTCACCA GGGACCTCACCA 0 19 4.32 5.14E−03 3′ss CLL 43522984-43527983 43523029-43527983 AGCGCCCGCCCC AGCGCCCGATCT TCATCAACCTGC GCAGGCAGGCCC AGAT (552) TGAA (553) 306 chr9: chr9: CCAAGGACTGCA CCAAGGACTGCA 2 57 4.27 1.96E−04 3′ss CLL 139837449-139837800 139837395-139837800 CTGTGAAGGCCC CTGTGAAGATCT CCGCCCCGCGAC GGAGCAACGACC CTGG (175) TGAC (176) 307 chr4: chr4: GAGTGTGAATCA GAGTGTGAATCA 2 56 4.25 3.01E−02 3′ss CLL 56874548-56875878 56874548-56875900 TCTGTGAATTTC TCTGTGAACCAG ACATCACTCATT CTGAAAGAAACA TAAC (554) TTGG (555) 308 chr5: chr5: AGCATTGCTAGA AGCATTGCTAGA 1 37 4.25 3.83E−05 3′ss CLL 139815842-139818078 139815842-139818045 AGCAGCAGCTTT AGCAGCAGGAAT TGCAGATCCTGA TGGCAAATTGTC GGTA (19) AACT (20) 309 chr22: chr22: TCATCAATGCCC TCATCAATGCCC 0 18 4.25 3.60E−04 3′ss CLL 24204389-24209938 24204389-24210667 CGACCTTGGTTC CGACCTTGCACA ATGAACACATTG TTCAGGAATTCA AGGT (556) CCAA (545) 310 chr3: chr3: GCATTTCTGAGA GCATTTCTGAGA 0 18 4.25 3.30E−03 3′ss CLL 38038678-38038959 38038678-38038973 AGGCTCGGGTCC AGGCTCGGGGGC TCTCCCGCAGGG TGGCTTTGACCT GCTG (557) ACAG (558) 311 chr6: chr6: GCCAGTCCAGAG GCCAGTCCAGAG 1 36 4.21 6.38E−07 3′ss CLL 109767078-109767338 109767065-109767338 CCCTCAAGTTCT CCCTCAAGCTCT TCTTCTCAGCTC TGTGGCCATGGA TTGT (559) GAAG (560) 312 chr1: chr1: TGGCCGAGGCGC TGGCCGAGGCGC 2 54 4.20 1.35E−04 3′ss CLL 16803042-16803424 16802999-16803424 TGACCAAGACCT TGACCAAGGCTG TACTCAGGGGAT AGGGCAGAGGAG CCTC (561) GCCT (562) 313 chr2: chr2: TCTACTTGGTGG TCTACTTGGTGG 3 72 4.19 1.68E−06 3′ss CLL 103348885-103353104 103348868-103353104 GCTTCTTGCATT GCTTCTTGGATT TATTTTGTTTTA TGTTTGGTGTCA GGAT (563) GCAT (564) 314 chr14: chr14: GCTCCTGCTCAG GCTCCTGCTCAG 0 17 4.17 3.99E−04 3′ss CLL 78203438-78205120 78203418-78205120 TATATCCGTTTT TATATCCGATAC TATCTGCTTTCT ACACCATCTCAG TCAG (565) CAAG (566) 315 chr3: chr3: GAAATAGGGCAC GAAATAGGGCAC 0 17 4.17 7.71E−03 3′ss CLL 122152652-122156016 122152635-122156016 AGATCCAGTTTT AGATCCAGACTG TCTTTAATTTTA TGATAGATGCCA GACT (567) ACAT (568) 316 chr18: chr18: GCAACCTGTGTT GCAACCTGTGTT 1 33 4.09 3.11E−03 3′ss CLL 33724997-33725896 33724997-33725910 TTACAAAGGTTT TTACAAAGATGG TATTTTTTAGAT TGTCCTACAGCA GGTG (569) GCCA (570) 317 chr7: chr7: GTATCAAAGTGT GTATCAAAGTGT 1 33 4.09 4.37E−04 3′ss CLL 94157562-94162500 94157562-94162516 GGACTGAGATTT GGACTGAGGATT GTCTTCCTTTAG CCATTGCAAAGC GATT (27) CACA (28) 318 chr4: chr4: CCCCTGAAGTAC CCCCTGAAGTAC 0 16 4.09 1.12E−04 3′ss CLL 39868635-39871013 39868617-39871013 TAGCAAAGCATG TAGCAAAGGTAC TTAATATTTTAT AGGCAATTAAAC AGGT (571) TTCT (572) 319 chr10: chr10: GTTCCTCACTTT GTTCCTCACTTT 1 31 4.00 1.17E−04 3′ss CLL 99502921-99504468 99502921-99504485 GAATGAGGTGTT GAATGAGGGTGC TTTGATTCTGCA ATGGTACTCAGT GGTG (573) AGGT (574) 320 chr1: chr1: TCAGCCCTCTGA TCAGCCCTCTGA 0 15 4.00 6.99E−03 3′ss CLL 226036315-226036597 226036255-226036597 ACTACAAAGGTG ACTACAAAACAG TTTGTTCACAGA AAGAGCCTGCAA GATC (93) GTGA (94) 321 chr20: chr20: TCTTGGAAGGCA TCTTGGAAGGCA 0 15 4.00 4.25E−03 3′ss CLL 31983014-31984566 31982922-31984566 GAGAAAAGATAT GAGAAAAGTCTA TTCTAGAGCATT CCTCGAGACCTA TGGG (575) TGGC (576) 322 chr2: chr2: AACCCGGAGAGA AACCCGGAGAGA 0 15 4.00 5.64E−03 3′ss CLL 64456774-64456978 64456774-64478252 AAAGGGAGTTTG AAAGGGAGCAAC TTTTTAGGTCAG TGATGTTGCCAT AGTC (577) GCAG (578) 323 chr11: chr11: AATCTTCCCCAA AATCTTCCCCAA 1 30 3.95 7.37E−04 3′ss CLL 92887382-92895871 92887443-92895871 GATGTATGTTCT GATGTATGGTTA ATGTTCCAGCAG TATCAATCAGTG AGAT (579) AAAA (580) 324 chr18: chr18: CTCTCTTGTCAG CTCTCTTGTCAG 1 30 3.95 2.23E−02 3′ss CLL 43459192-43460039 43459179-43460039 ACAAGCAGTTGT ACAAGCAGGTAA CTCTTCCAGGTA TGGAGACTATAC ATGG (581) AGTG (582) 325 chr5: chr5: GCAGAGCTGTGG GCAGAGCTGTGG 1 30 3.95 1.23E−03 3′ss CLL 138724290-138725368 138724274-138725368 CTTACCAGTCCC CTTACCAGATGT TCCTTGTTCCAG GGCAAAATCTGG ATGT (583) CAAA (584) 326 chr17: chr17: TGCAGGAGACCG TGCAGGAGACCG 1 29 3.91 7.83E−03 3′ss CLL 58163509-58165557 58163487-58165557 GCTTTTGGGTCC GCTTTTGGATAC CCTTCTTATACC TGCTAATCAGTC CCTC (585) CTAG (586) 327 chr1: chr1: AGTTACAACGAA AGTTACAACGAA 1 29 3.91 2.95E−05 3′ss CLL 185056772-185060696 185056772-185060710 CACCTCAGTGAC CACCTCAGGAGG TCTTTTACAGGA CAATAACAGATG GGCA (162) GCTT (163) 328 chr10: chr10: TCTTGCCAGAGC TCTTGCCAGAGC 0 14 3.91 5.04E−05 3′ss CLL 99219232-99219415 99219283-99219415 TGCCCACGCTCT TGCCCACGCTTC CCACCCTCAGCT TTTCCTTGCTGC GCCT (587) TGGA (588) 329 chr4: chr4: CCATGGTCAAAA CCATGGTCAAAA 0 14 3.91 4.36E−02 3′ss CLL 152022314-152024139 152022314-152024022 AATGGCAGCACC AATGGCAGACAA AACAGGTCCGCC TGATTGAAGCTC AAAT (344) ACGT (345) 330 chr1: chr1: ATCAGAAATTCG ATCAGAAATTCG 3 57 3.86 4.89E−06 3′ss CLL 212515622-212519131 212515622-212519144 TACAACAGGTTT TACAACAGCTCC CTTTTAAAGCTC TGGAGCTTTTTG CTGG (65) ATAG (66) 331 chr1: chr1: GCAGGCTGCCCG GCAGGCTGCCCG 4 69 3.81 2.04E−07 3′ss CLL 156552962-156553113 156552962-156553129 GGACTCTGGCTC GGACTCTGGGGA TCTTTCTCTCAG CATGAAGGGACA GGGA (589) GTGG (590) 332 chr6: chr6: GCCAGTCCAGAG GCCAGTCCAGAG 2 41 3.81 4.40E−03 3′ss CLL 109767165-109767338 109767065-109767338 CCCTCAAGTCTT CCCTCAAGCTCT TACCAGACTTGC TGTGGCCATGGA AGGG (591) GAAG (560) 333 chr20: chr20: ACATGAAGGTGG ACATGAAGGTGG 5 81 3.77 1.48E−08 3′ss CLL 34144042-34144725 34144042-34144743 ACGGAGAGGCTC ACGGAGAGGTAC CCCTCCCACCCC TGAGGACAAATC AGGT (49) AGTT (50) 334 chr17: chr17: CTATTTCACTCT CTATTTCACTCT 1 25 3.70 2.79E−05 3′ss CLL 7131030-7131295 7131102-7131295 CCCCCGAACCTA CCCCCGAAATGA TCCAGGTTCCTC GCCCATCCAGCC CTCC (33) AATT (34) 335 chr6: chr6: TTCCCACTGGTC TTCCCACTGGTC 1 25 3.70 3.91E−03 3′ss CLL 110085185-110086201 110085185-110086215 GCCTGCAGGTAT GCCTGCAGACTG TTCTCTTTAGAC GCATCCTTCGAA TGGC (592) CCAA (593) 336 chr7: chr7: TGTAAATGGGGA TGTAAATGGGGA 1 25 3.70 2.18E−05 3′ss CLL 889240-889468 889240-889559 AGCGCTGTTTTC AGCGCTGTGCGA TACAGACTGCCA CGACTGTAAGGG TTGC (594) CAAG (595) 337 chr12: chr12: TCAATGCAAATA TCAATGCAAATA 0 12 3.70 1.92E−03 3′ss CLL 112915534-112915638 112915534-112915660 TCATCATGGATT TCATCATGCCTG TTCTTCCTAAAT AATTTGAAACCA TTCT (596) AGTG (597) 338 chr14: chr14: ACAAATCAACTG ACAAATCAACTG 0 12 3.70 1.38E−03 3′ss CLL 56100059-56101230 56100059-56101243 GAAAGCAATTAC GAAAGCAAGCAG TGTTTTCAGGCA TCTGCAGAACTA GTCT (598) AATA (599) 339 chr17: chr17: CAAAGCGCCCAG CAAAGCGCCCAG 0 12 3.70 2.10E−02 3′ss CLL 2266428-2266727 2266428-2266758 CCCTGGGGGCTG CCCTGGGGATCC GAGGCTGAGCCC GGAAACGGCACT CGGC (600) CAAG (601) 340 chr19: chr19: TGACACAGCCCT TGACACAGCCCT 0 12 3.70 4.53E−05 3′ss CLL 16264018-16265158 16264018-16265208 GCAGGCAGGACC GCAGGCAGAAGG TTTCCCCCTCCC ATCCCGCAAACG TAGT (602) TGGA (511) 341 chr1: chr1: AGTTGCCATTCC AGTTGCCATTCC 0 12 3.70 4.52E−03 3′ss CLL 186324917-186325417 186324900-186325417 ATTACATGTCTT ATTACATGCTTC TACTTTCCTGAA AAGCTTAGATGA GCTT (603) TGTT (604) 342 chr3: chr3: ACTGATTAAAAA ACTGATTAAAAA 4 62 3.66 9.33E−05 3′ss CLL 56649300-56649931 56649300-56649949 TCTTGGTGGTGA TCTTGGTGTTGA TTTCTCTTTGCC TACAATACAAAT AGTT (605) GGAA (606) 343 chr6: chr6: CCGGGGCCTTCG CCGGGGCCTTCG 4 58 3.56 3.53E−06 3′ss CLL 10723474-10724788 10723474-10724802 TGAGACCGCTTG TGAGACCGGTGC TTTTCTGCAGGT AGGCCTGGGGTA GCAG (95) GTCT (96) 344 chr3: chr3: AGGCTATTGTTG AGGCTATTGTTG 1 22 3.52 2.36E−03 3′ss CLL 184587316-184588487 184587316-184588503 CAGACCGGGCTG CAGACCGGATGG TTTTCCTTACAG TAGAAATCCTAT ATGG (607) TCCA (608) 345 chr4: chr4: CCTTTCAAGAAA CCTTTCAAGAAA 1 22 3.52 1.60E−02 3′ss CLL 3124663-3125976 3124663-3127275 ACAAAAAGTCGC ACAAAAAGGCAA TTTTTCCAGTGG AGTGCTCTTAGG CGGT (609) AGAA (610) 346 chr9: chr9: ACACGGAGCTCA ACACGGAGCTCA 2 33 3.50 1.45E−05 3′ss CLL 123933826-123935634 123933826-123935520 AGAAACAGTTTC AGAAACAGATGG TTCCAGAACTAC CAAACCAAAAAG CAGC (611) ATTT (612) 347 chr19: chr19: CAAGCAGGTCCA CAAGCAGGTCCA 6 76 3.46 9.28E−05 3′ss CLL 5595521-5598803 5595508-5598803 AAGAGAGATTTT AAGAGAGAAGCT GGTAAACAGAGC CCAAGAGTCAGG TCCA (138) ATCG (139) 348 chr5: chr5: GACTTCGAACAT GACTTCGAACAT 4 54 3.46 7.66E−03 3′ss CLL 78608321-78610192 78608321-78610079 TTAAACAGTGTG TTAAACAGAGGT TTACAGGTAGAA ATCCTGGGCAAG GAGA (613) TCAT (614) 349 chr2: chr2: ACCACGAAGGGT ACCACGAAGGGT 2 32 3.46 1.25E−02 3′ss CLL 231050873-231065600 231050859-231065600 CACACAAGTCTA CACACAAGGGGC TTTGGTCCAGGG AGCCTCACCTGG GCAG (615) GCAT (616) 350 chr1: chr1: CGATCTCCCAAA CGATCTCCCAAA 1 21 3.46 1.57E−05 3′ss CLL 52880319-52880412 52880319-52880433 AGGAGAAGTCTG AGGAGAAGCCCC ACCAGTCTTTTC TCCCCTCGCCGA TACA (55) GAAA (56) 351 chr2: chr2: TTAACAAACACG TGCTGGCACACC 0 10 3.46 8.22E−03 5′ss CLL 69015785-69034404 69015088-69034404 TGAATCTACAGT CTGTGGAGCAGT GTTTGGCCAGCG GTTTGGCCAGCG CTTG (617) CTTG (618) 352 chr5: chr5: CGCCCCAGGGCA CGCCCCAGGGCA 0 10 3.46 1.97E−03 3′ss CLL 156915521-156916109 156915497-156916109 AGCGAAAGGTGT AGCGAAAGGTGA TCCTTGACTTGT TCAACACTCCGG GCGT (619) AAAT (620) 353 chr9: chr9: TGGTACAACTTC TGGTACAACTTC 0 10 3.46 6.70E−03 3′ss CLL 115934002-115935732 115933986-115935732 AGGAAAAGTCTG AGGAAAAGTGTT TTTGTTTTGCAG TAGCCCTCCAGG TGTT (621) CCCA (622) 354 chr14: chr14: TGGATTTGCTCG TGGATTTGCTCG 1 20 3.39 1.52E−04 3′ss CLL 50808004-50808849 50807950-50808849 GCTTTTGATTTT GCTTTTGACTGG GATTCCAGCCTT ACCGAGTGACTA CCGC (623) CTAT (624) 355 chr18: chr18: GATGAGGACCCC GATGAGGACCCC 5 61 3.37 3.06E−06 3′ss CLL 9133520-9136361 9133508-9136361 CACATAGGTTTC CACATAGGGATG CAAACCAGGATG GCCATAGCAGCC GCCA (625) ACAA (626) 356 chr10: chr10: TACCTCTGGTTC TACCTCTGGTTC 3 39 3.32 2.21E−05 3′ss CLL 99214556-99215395 99214556-99215416 CTGTGCAGTCTT CTGTGCAGTTCT CGCCCCTCTTTT GTGGCACTTGCC CTTA (13) CTGG (14) 357 chr2: chr2: TGTTTTAAATTC TGTTTTAAATTC 2 29 3.32 8.44E−06 3′ss CLL 225670231-225670842 225670246-225670842 CATAGCAGCTAT CATAGCAGCATT TTCTACAGTAAA TTCATCAATAGC CCAT (627) TATT (628) 358 chrX: chrX: GCTGGGATGTTA GCTGGGATGTTA 1 19 3.32 2.06E−02 3′ss CLL 153323986-153357641 153298008-153357641 GGGCTCAGCCTG GGGCTCAGGGAA TCGTTCCAGGAC GAAAAGTCAGAA CCAG (629) GACC (630) 359 chr16: chr16: CTGGTTATTGCA CTGGTTATTGCA 0 9 3.32 6.10E−05 3′ss CLL 72139523-72139882 72139523-72139903 AATTAAAGCTCT AATTAAAGGTCT TTGCCGTCCCCT TCAACCCCAGGA CCTA (631) TTGG (632) 360 chr5: chr5: CTCCATGCTCAG CTCCATGCTCAG 4 48 3.29 1.01E−06 exon CLL 869519-870587 865696-870587 CTCTCTGGTTTC CTCTCTGGGGAA incl. TTTCAGGGCCTG GGTGAAGAAGGA CCAT (128) GCTG (129) 361 chrX: chrX: GGTCATGCTAAT GGTCATGCTAAT 8 82 3.21 5.22E−07 3′ss CLL 70516897-70517210 70516897-70517226 GAGACAGGTCTG GAGACAGGATTT TTGTTTTTTTAG GATGAGGCGCCA ATTT (633) AGAA (634) 362 chr16: chr16: GTCAGCATTTGC GTCAGCATTTGC 2 26 3.17 7.43E−04 3′ss CLL 47347747-47399698 47347734-47399698 AGACTTTGTTTC AGACTTTGATGG TTTTGGCAGATG AGATGGACACAT GAGA (635) GGAT (636) 363 chr5: chr5: GCAGAGCTGTGG GCAGAGCTGTGG 2 26 3.17 1.17E−03 3′ss CLL 138725125-138725368 138724274-138725368 CTTACCAGACTT CTTACCAGATGT CTCCCTTTCCAG GGCAAAATCTGG GCCC (637) CAAA (584) 364 chr11: chr11: CGGCGCGGGCAA CGGCGCGGGCAA 0 8 3.17 6.70E−03 3′ss CLL 62648919-62649352 62648919-62649364 CCTGGCGGCCCC CCTGGCGGGTCT CATTTCAGGTCT GAAGGGGCGTCT GAAG (165) CGAT (166) 365 chr11: chr11: TGCAGCTGGCCC TGCAGCTGGCCC 0 8 3.17 2.22E−02 3′ss CLL 64002365-64002911 64002365-64002929 CCGCCCAGGTCT CCGCCCAGGCCC TTTCTCTCCCAC CTGTCTCCCAGC AGGC (638) CTGA (639) 366 chr14: chr14: CACAGCAAGCAC CACAGCAAGCAC 0 8 3.17 3.01E−05 3′ss CLL 31169464-31171484 31169464-31171501 CTTCTGAGTTCT CTTCTGAGGCTG TTTCTTATTTCA ATTTGGAGCAAT GGCT (640) ATAA (641) 367 chr1: chr1: TCACACCTGTAG TCACACCTGTAG 0 8 3.17 9.33E−05 3′ss CLL 186300728-186301326 186300713-186301326 GAACTGAGTGTA GAACTGAGGAAG TTATGATACAGG AAGTTATGGCAG AAGA (642) AAGA (643) 368 chr5: chr5: AAAATTGACTAT AAAATTGACTAT 0 8 3.17 7.30E−03 3′ss CLL 169101449-169108733 169101449-169108747 GGCAACAATTTT GGCAACAAAATC TGCTTTACAGAA CTTGAGCTTGAT TCCT (644) TTGA (645) 369 chr9: chr9: ACACGGAGCTCA ACACGGAGCTCA 0 8 3.17 5.42E−04 3′ss CLL 123933826-123935644 123933826-123935520 AGAAACAGAACT AGAAACAGATGG ACCAGCAGATCT CAAACCAAAAAG AGAA (646) ATTT (612) 370 chr10: chr10: GGGAGGAAAAGT GGGAGGAAAAGT 5 52 3.14 1.27E−03 3′ss CLL 112058568-112060304 112058548-112060304 AATTAATGTTTT AATTAATGGAAG TGTTTTTCTTTT TTATAGAACTAA TTAG (647) CCAA (648) 371 chr3: chr3: ATTTGGATCCTG ATTTGGATCCTG 4 43 3.14 1.46E−04 3′ss CLL 196792335-196792578 196792319-196792578 TGTTCCTCTTTT TGTTCCTCATAC TTTCTGTTAAAG AACTAGACCAAA ATAC (87) ACGA (88) 372 chr12: chr12: ATTTGGACTCGC ATTTGGACTCGC 3 34 3.13 1.20E−04 3′ss CLL 105601825-105601935 105601807-105601935 TAGCAATGATGT TAGCAATGAGCA CTGTTTATTTTT TGACCTCTCAAT AGAG (41) GGCA (42) 373 chr19: chr19: CTATGGGCTCAC CTATGGGCTCAC 7 67 3.09 2.90E−04 3′ss CLL 41084118-41084353 41084118-41084367 TCCTCTGGTCCT TCCTCTGGTTCG CCTGTTGCAGTT TCGCCTGCAGCT CGTC (169) TCGA (170) 374 chr11: chr11: TTCTCCAGGACC TTCTCCAGGACC 1 16 3.09 4.69E−03 3′ss CLL 125442465-125445146 125442465-125445158 TTGCCAGACCTT TTGCCAGAGGAA TTCTATAGGGAA TCAAAGACTCCA TCAA (150) TCTG (151) 375 chr12: chr12: AGAAGGAGCTGC AGAAGGAGCTGC 1 16 3.09 2.88E−03 3′ss CLL 110437589-110449795 110437589-110449809 AGGGCCAGTGTT AGGGCCAGAATG TCCTTCACAGAA TGGAGGCTGTGG TGTG (649) ACCC (650) 376 chr8: chr8: GCTCTGGAGAAT GCTCTGGAGAAT 4 41 3.07 6.90E−07 3′ss CLL 126051218-126052036 126051201-126052036 CTCAATAAGGTT CTCAATAAGGCT TTTCTTCCTTTA CTCCTAGCAGAC GGGC (651) ATTG (652) 377 chr3: chr3: CATGCAATGAAC CATGCAATGAAC 2 24 3.06 7.00E−06 3′ss CLL 42674315-42675109 42674315-42675071 CCAAAAGGTTGA CCAAAAGGTCAC TTCCAGTGCTAA TCTGAGAGGAGT AAGG (653) GATA (654) 378 chr5: chr5: TGCTTCCGGAAC TGCTTCCGGAAC 6 57 3.05 3.26E−05 3′ss CLL 139941307-139941428 139941286-139941428 AGTGACAGCCCC AGTGACAGGGAC ATCTCTGCCCCT TTCGCTTTTGTG GCTA (655) GCAA (656) 379 chr12: chr12: TGGGTTTCAGCA TGGGTTTCAGCA 0 7 3.00 4.31E−03 3′ss CLL 64199184-64202434 64199184-64202454 AGAGAACATTGT AGAGAACACTGG TTTTCTGATTTT CAGCCTCAGGAA CTAG (657) ACAA (658) 380 chr18: chr18: AGGACATGGATT AGGACATGGATT 0 7 3.00 4.13E−03 3′ss CLL 47311742-47313660 47311721-47313660 TGGTAGAGTGCT TGGTAGAGGTGA CTAATTTTTGTT ATGAAGCTTTTG TTAA (659) CTCC (660) 381 chr19: chr19: ATCACAACCGGA ATCACAACCGGA 0 7 3.00 2.46E−02 3′ss CLL 15491444-15507960 15491423-15507960 ACCGCAGGCTCC ACCGCAGGCTCA TTCTGCCCTGCC TGATGGAGCAGT CGCA (661) CCAA (662) 382 chr1: chr1: CAGGAAGCAGCT CAGGAAGCAGCT 0 7 3.00 7.09E−04 3′ss CLL 46068037-46070588 46068037-46070607 AGTCTTTTATGT AGTCTTTTAGGT TTATTCTCTTTG AAGAAGTATGGA TAGA (663) GAGA (664) 383 chr21: chr21: GAACCAATGGAA GAACCAATGGAA 0 7 3.00 1.40E−02 3′ss CLL 45452053-45452682 45452053-45457672 TGGAGAAGGCAC TGGAGAAGGTCC AGGCGTTTTGCA TATGGCCGGGCT AAGG (665) CCGA (666) 384 chr2: chr2: TGCTTGTAAAAT TGCTTGTAAAAT 0 7 3.00 1.13E−02 3′ss CLL 160673561-160676236 160673543-160676236 TGAAATGGTGCT TGAAATGGTTGA TTTAATTATTAT CTACAAAGAAGA AGTT (667) ATAT (668) 385 chr5: chr5: ACTCGCGCCTCT ACTCGCGCCTCT 0 7 3.00 4.59E−02 3′ss CLL 150411955-150413168 150411944-150413168 TCCATCTGTTTT TCCATCTGCCGG GTCGCAGCCGGA AATACACCTGGC ATAC (109) GTCT (110) 386 chr7: chr7: CCACCTCACCAT CCACCTCACCAT 0 7 3.00 2.08E−02 3′ss CLL 99954506-99955853 99954506-99955842 CACCCAGGCCCC CACCCAGGCCCT TCCACAGGGCCC CAGGCAGCCCCT CTCT (669) CCAC (515) 387 chr4: chr4: CGTCTCCATGAC CGTCTCCATGAC 6 54 2.97 7.33E−05 3′ss CLL 995351-995438 995351-995466 CATGCAAGGTGT CATGCAAGGCTT AGACGCAGTGCT CCTGAACTACTA CCCC (670) CGAT (671) 388 chr15: chr15: AGGAGGCAATTA AGGAGGCAATTA 8 68 2.94 1.81E−04 3′ss CLL 75131104-75131350 75131086-75131350 AGGCAAAGGCCC AGGCAAAGGTGG TTTCCCTGCTAC GGCAGTACGTGT AGGT (672) CCCG (673) 389 chrX: chrX: TACAAGAGCTGG TACAAGAGCTGG 2 22 2.94 1.26E−04 3′ss CLL 153699660-153699819 153699660-153699830 GTGGAGAGGGTC GTGGAGAGGTAT CCAACAGGTATT TATCGAGACATT ATCG (158) GCAA (159) 390 chr9: chr9: CACCACGCCGAG CACCACGCCGAG 5 43 2.87 3.76E−08 3′ss CLL 125023777-125026993 125023787-125026993 GCCACGAGACAT GCCACGAGTATT TGATGGAAGCAG TCATAGACATTG AAAC (142) ATGG (143) 391 chr14: chr14: TTACCTCCGAAG TTACCTCCGAAG 10 79 2.86 3.40E−05 3′ss CLL 23242937-23243141 23242925-23243141 GATCGTGGTTCT GATCGTGGGGTC CTTTGTAGGGTC TGCCACAAGGTA TGCC (674) CCTC (675) 392 chr11: chr11: AATAAGCCCTCA AATAAGCCCTCA 0 6 2.81 1.66E−02 3′ss CLL 67376193-67376896 67376193-67376922 GATGGCAGCCTG GATGGCAGGCCC TCTGACCTGTGG AAGTATCTGGTG GCCC (676) GTGA (677) 393 chr16: chr16: ACTCCCAGCTCA ACTCCCAGCTCA 0 6 2.81 1.49E−02 3′ss CLL 56403209-56419830 56403239-56419830 ATGCAATGGTTC ATGCAATGGCTC CATACCATCTGG ATCAGATTCAAG TACT (332) AGAT (333) 394 chr17: chr17: GCCTGGACCTGT GCCTGGACCTGT 0 6 2.81 4.26E−02 3′ss CLL 43316432-43317875 43316432-43317842 ACTTGGAGGTGC ACTTGGAGAGGC AGATCCAGGCGT TTCGGCTCACCG ACCT (678) AGAG (679) 395 chr21: chr21: CTGTAACTACTA CTGTAACTACTA 0 6 2.81 3.47E−04 3′ss CLL 47655360-47656742 47655340-47656742 GCCCACAGTTTC GCCCACAGAGTG TTTTTTATTCAA ACATGATGAGGG ATAG (680) AGCA (681) 396 chr3: chr3: CTCTCAATGCAG CTCTCAATGCAG 0 6 2.81 1.49E−03 3′ss CLL 71019345-71019886 71015207-71019886 CTTTACAGTTTT CTTTACAGGCTT CCTGCAGATTGT CAATGGCTGAGA TCAA (682) ATAG (683) 397 chr9: chr9: GGAGCAGTTCCA GGAGCAGTTCCA 0 6 2.81 4.44E−03 3′ss CLL 95007367-95009658 95007353-95009658 GAAGACTGCTGC GAAGACTGGGAC TTCTCCATAGGG CATTGTTGTGGA ACCA (684) AGGC (685) 398 chrX: chrX: CCTGCTGGACCA CCTGCTGGACCA 0 6 2.81 1.25E−02 3′ss CLL 48340103-48340769 48340103-48340796 TTCTTACGTTGT TTCTTACGATTT CTCCCCCTGTTC CAACCAGCTGGA CTAA (686) TGGT (687) 399 chr20: chr20: GGATTTTGATAA GGATTTTGATAA 7 53 2.75 1.01E−03 3′ss CLL 36631195-36634598 36631178-36634598 TGAAGAAGTTGT TGAAGAAGAGGA GCTCTTTTTCCA ACAGTCAGTCCC GAGG (688) TCCC (689) 400 chr4: chr4: CGTCTCCATGAC CGTCTCCATGAC 3 26 2.75 5.89E−04 3′ss CLL 995351-995433 995351-995466 CATGCAAGGGCA CATGCAAGGCTT GGTGTAGACGCA CCTGAACTACTA GTGC (690) CGAT (671) 401 chr15: chr15: TGATTCCAAGCA TGATTCCAAGCA 2 19 2.74 3.63E−05 3′ss CLL 25213229-25219533 25213229-25219457 AAAACCAGCCTT AAAACCAGGCTC CCCCTAGGTCTT CATCTACTCTTT CAGA (230) GAAG (231) 402 chr18: chr18: AGTGCCAGCTGC AGTGCCAGCTGC 2 19 2.74 1.04E−03 exon CLL 47811617-47812118 47811721-47812118 GGGCCCGGCTCT GGGCCCGGGAAT skip CACCAGTGACGC CGTACAAGTACT CCTC (691) TCCC (692) 403 chr18: chr18: AACTTACTTTGT AACTTACTTTGT 2 19 2.74 1.46E−04 3′ss CLL 66356291-66358531 66355002-66358531 TTATGATGCTTT TTATGATGAGTA TATTTTAGATTC TGAAGATGGTGA AGAG (693) TCTG (694) 404 chr21: chr21: ATCATAGCCCAC ATCATAGCCCAC 3 25 2.70 2.17E−02 3′ss CLL 37416267-37417879 37416254-37417879 ATGTCCAGTTTT ATGTCCAGGTAA TCTTTCTAGGTA AAGCAGCGTTTA AAAG (695) ATGA (696) 405 chrX: chrX: TGACTCCGCTGC TGACTCCGCTGC 1 12 2.70 2.07E−02 3′ss CLL 118923962-118925536 118923974-118925536 TCGCCATGACTT TCGCCATGTCTT TCAGGATTAAGC CTCACAAGACTT GATT (697) TCAG (698) 406 chr1: chr1: CCAAGCACCTGA CCAAGCACCTGA 7 50 2.67 1.87E−03 3′ss CLL 100606070-100606400 100606070-100606522 AACAGCAGTTTG AACAGCAGATGC CAGGCTTCTATT TGAAAAAGTTCA TTAG (699) CTTC (700) 407 chr12: chr12: GCCTGCCTTTGA GCCTGCCTTTGA 13 88 2.67 1.74E−07 3′ss CLL 113346629-113348840 113346629-113348855 TGCCCTGGATTT TGCCCTGGGTCA TGCCCGAACAGG GTTGACTGGCGG TCAG (71) CTAT (72) 408 chr7: chr7: CGAGCTGTTGGC CGAGCTGTTGGC 7 49 2.64 2.27E−05 3′ss CLL 149547427-149549949 149547427-149556510 ATCCTTGGTTTC ATCCTTGGGACC TTGTCCACAGGA TGCCGCTGCCAA GAAG (701) GCCA (702) 409 chr11: chr11: GCTTTCTACGGA GCTTTCTACGGA 3 24 2.64 1.08E−04 3′ss CLL 126142974-126143210 126142974-126143230 ACATCAATGAGC ACATCAATGAGT TTCTGTCTGCAC ACCTGGCCGTAG ACAG (703) TCGA (704) 410 chr8: chr8: TTATTTTACACA TTATTTTACACA 3 24 2.64 2.89E−05 3′ss CLL 38095145-38095624 38095145-38095606 ATCCAAAGCCAG ATCCAAAGCTTA TTGCAGGGTCTG TGGTGCATTACC ATGA (57) AGCC (58) 411 chr12: chr12: CAGGAATACCTG CAGGAATACCTG 1 11 2.58 2.06E−06 3′ss CLL 62783294-62783413 62783294-62783384 CAGATAAGATTT CAGATAAGATGA CACAGAATATTC TAGTTACTGATA GCTA (705) TATA (706) 412 chr17: chr17: CTACACCAAGAA CTACACCAAGAA 1 11 2.58 2.56E−03 3′ss CLL 18007203-18007857 18007203-18007936 GAGAGGACCTCT GAGAGGACAGAG TCCCTCGCGCAG GCCAGACTTCAC AATC (707) AGAC (708) 413 chr17: chr17: CGGAGGCTGTCT CGGAGGCTGTCT 1 11 2.58 4.39E−03 3′ss CLL 73486839-73487110 73486839-73487129 CCTCTCAGACTT CCTCTCAGGAAA CCTCTCTCCCAC TGCTGCGCTGCA CAGG (709) TTTG (710) 414 chr11: chr11: TCCTGCTGGAGC TCCTGCTGGAGC 0 5 2.58 5.77E−03 3′ss CLL 68331900-68334466 68331900-68334481 CACCCAAGCTTT CACCCAAGAAAA TTCTTCTTCAGA GTGTGATGAAGA AAAG (711) CCAC (712) 415 chr13: chr13: AGCTGAAATTTC AGCTGAAATTTC 0 5 2.58 3.85E−02 3′ss CLL 113915073-113917776 113915073-113917800 CAGTAAAGGGGG CAGTAAAGCCTG GTTTTATTCTTC GAGATTTGAAAA TTTT (152) AGAG (153) 416 chr13: chr13: ACCAAGCATACT ACCAAGCATACT 0 5 2.58 1.04E−02 3′ss CLL 20656270-20656905 20656270-20656920 TCCAGATGTTCT TCCAGATGGGTC CTCTATTTAAGG AATATTCTCTCG GTCA (713) AGTT (714) 417 chr19: chr19: CGGGCCGCCCCC CGGGCCGCCCCC 0 5 2.58 1.76E−03 3′ss CLL 36231397-36231924 36230989-36231924 CTGCCCGGTGTT CTGCCCGGAGGC CTTCTGGGCAGT CGGTCCCTGCCA GCAA (715) AGGG (716) 418 chr20: chr20: ACATGAAGGTGG ACATGAAGGTGG 0 5 2.58 3.36E−03 3′ss CLL 34144042-34144761 34144042-34144743 ACGGAGAGTTCT ACGGAGAGGTAC CTGTGACCAGAC TGAGGACAAATC ATGA (250) AGTT (50) 419 chr21: chr21: AAGATGTCCCTG AAGATGTCCCTG 0 5 2.58 3.03E−02 3′ss CLL 38570326-38572514 38570326-38572532 TGAGGATTGTGT TGAGGATTGCAC GTTTGTTTCCAC TGGGTGCAAGTT AGGC (224) CCTG (225) 420 chr6: chr6: GGAGGACTGGGG GGAGGACTGGGG 0 5 2.58 2.97E−03 3′ss CLL 32095539-32095893 32095527-32095893 TCTGCAGACATT TCTGCAGAACAG TCTTGCAGACAG CACCTTGTATTC CACC (717) TGGC (718) 421 chr7: chr7: CTGCCCCCTGCG CTGCCCCCTGCG 0 5 2.58 7.48E−03 3′ss CLL 44795898-44796008 44795898-44796023 CCACACGGCCTC CCACACGGTGAT TTTCCCTGCAGT GGTTCATTCGCA GATG (719) TATG (720) 422 chr7: chr7: TGTAAATGGGGA TGTAAATGGGGA 0 5 2.58 2.68E−02 3′ss CLL 889240-889477 889240-889559 AGCGCTGTACTG AGCGCTGTGCGA CCATTGCTATGC CGACTGTAAGGG ACGG (721) CAAG (595) 423 chr12: chr12: GGCCAGCCCCCT GGCCAGCCCCCT 10 62 2.52 1.37E−08 3′ss CLL 120934019-120934204 120934019-120934218 TCTCCACGGCCT TCTCCACGGTAA TGCCCACTAGGT CCATGTGCGACC AACC (206) GAAA (207) 424 chr9: chr9: CTGATGAAAACT CTGATGAAAACT 11 66 2.48 1.51E−04 3′ss CLL 93641235-93648124 93641235-93650030 ACTACAAGCAGA ACTACAAGGCCC CACCTTACAGGC AGACCCATGGAA CAGG (722) AGTG (723) 425 chr17: chr17: TTCAGCTGCCCC TTCAGCTGCCCC 8 49 2.47 1.42E−05 3′ss CLL 57079102-57089688 57079075-57089688 TGAAGAAGAAAC TGAAGAAGGAAT ATGTTCTCCTTC GAGTAGCGACAG CTTC (724) TGAC (725) 426 chr15: chr15: GAAACCAACTAA GAAACCAACTAA 3 21 2.46 9.18E−03 3′ss CLL 59209219-59224554 59209198-59224554 AGGCAAAGCCCA AGGCAAAGGTAA TTTTCCTTCTTT AAAACATGAAGC CGCA (101) AGAT (102) 427 chr7: chr7: TCCCGAAGCCAC TCCCGAAGCCAC 3 21 2.46 4.67E−04 3′ss CLL 99752804-99752884 99752787-99752884 CTCATGAGCCTC CTCATGAGGTCG TGCCTTCCCCCA GGCAGTGTGATG GGTC (726) GAGC (727) 428 chr8: chr8: CCCCGGTGCGTA CCCCGGTGCGTA 1 10 2.46 2.22E−02 3′ss CLL 145624052-145624168 145624028-145624168 AGGAGGAGCCTG AGGAGGAGGAGG CCCCCCTTTGGC ACAATCCCAAGG CCTG (728) GGGA (729) 429 chr9: chr9: AGCTGGAGAAAA AGCTGGAGAAAA 1 10 2.46 3.34E−04 3′ss CLL 123932094-123935634 123932094-123935520 ACCTTCTTTTTC ACCTTCTTATGG TTCCAGAACTAC CAAACCAAAAAG CAGC (730) ATTT (731) 430 chr15: chr15: TTCGTTGGCAGC TTCGTTGGCAGC 6 37 2.44 2.59E−04 3′ss CLL 77327904-77328151 77327904-77328142 TTCTGCTGAGAC TTCTGCTGCGTC CCTGACCCCCAC CACAGAGACCCT CCCC (732) GACC (733) 431 chr19: chr19: GTGCTTGGAGCC GTGCTTGGAGCC 5 31 2.42 4.69E−03 3′ss CLL 55776746-55777253 55776757-55777253 CTGTGCAGACTT CTGTGCAGCCTG TCCGCAGGGTGT GTGACAGACTTT GCGC (179) CCGC (180) 432 chr4: chr4: GTGCCAACGAGG GTGCCAACGAGG 10 57 2.40 1.64E−03 3′ss CLL 184577127-184580081 184577114-184580081 ACCAGGAGTTCT ACCAGGAGATGG TTATTTCAGATG AACTAGAAGCAT GAAC (734) TACG (735) 433 chr16: chr16: CCTCACGATGCA CCTCACGATGCA 7 40 2.36 8.53E−04 3′ss CLL 67692735-67692830 67692719-67692830 AGGCCACGAGTT AGGCCACGGGAG CATGTCCCACAG AAGCTGTGTACA GGAG (736) CTGT (737) 434 chr6: chr6: AGGGGGCTCTTT AGGGGGCTCTTT 14 75 2.34 3.51E−06 3′ss CLL 91269953-91271340 91269933-91271340 ATATAATGTTTG ATATAATGTGCT TGCCTTTCTTTC GCATGGTGCTGA GCAG (265) ACCA (266) 435 chr15: chr15: TCACACAGGATA GCCTCACTGAGC 2 14 2.32 4.92E−03 exon CLL 25212299-25213078 25207356-25213078 ATTTGAAAGTGT AACCAAGAGTGT incl. CAGTTGTACCCG CAGTTGTACCCG AGGC (164) AGGC (145) 436 chr9: chr9: AAAAATAAAGCC CTGATGAAAACT 1 9 2.32 3.99E−03 5′ss CLL 93648256-93650030 93641235-93650030 TTTCCCAGGCCC ACTACAAGGCCC AGACCCATGGAA AGACCCATGGAA AGTG (738) AGTG (723) 437 chr14: chr14: CGAGGATGAAGA CGAGGATGAAGA 0 4 2.32 4.50E−03 3′ss CLL 34998676-35002649 34998681-35002649 CAGAGCAGGTGA CAGAGCAGTACA CCAAGAAAAAAA GGTGACCAAGAA AGAA (739) AAAA (740) 438 chr2: chr2: AGACAAGGGATT AGACAAGGGATT 0 4 2.32 1.21E−02 3′ss CLL 26437445-26437921 26437430-26437921 GGTGGAAACATT GGTGGAAAAATT TTATTTTACAGA GACAGCGTATGC ATTG (295) CATG (296) 439 chrX: chrX: AAAAGAAACTGA AAAAGAAACTGA 16 82 2.29 2.84E−08 3′ss CLL 129771378-129790554 129771384-129790554 GGAATCAGTATC GGAATCAGCCTT ACAGGCAGAAGC AGTATCACAGGC TCTG (303) AGAA (304) 440 chr1: chr1: TTCCCCATCAAC TTCCCCATCAAC 5 28 2.27 4.85E−06 3′ss CLL 19480448-19481411 19480433-19481411 ATCAAAAGTTTT ATCAAAAGTTCC GTTGTCTGCAGT AATGGTGGCAGT TCCA (202) AAGA (203) 441 chr3: chr3: AAAATGGGCTCA AAAATGGGCTCA 10 52 2.27 1.39E−04 3′ss CLL 141896447-141900302 141896418-141900302 GCAGTTAGGGTT GCAGTTAGACCT TTTTGTTGTTTG TTTCACAGATGC TTTG (741) TGCT (742) 442 chr1: chr1: AAGCACTGGCCC AAGCACTGGCCC 4 22 2.20 2.08E−02 3′ss CLL 156553242-156553591 156553242-156553588 AGTGTCAGGAGC AGTGTCAGAAGG CAGATTCTGTGC AGCCAGATTCTG GAGA (743) TGCG (744) 443 chr19: chr19: AGCCATTTATTT AGCCATTTATTT 11 53 2.17 2.14E−08 3′ss CLL 9728842-9730107 9728855-9730107 GTCCCGTGGGAA GTCCCGTGGGTT CCAATCTGCCCT TTTTTCCAGGGA TTTG (160) ACCA (161) 444 chr15: chr15: CCACTCTCACAA CCACTCTCACAA 1 8 2.17 1.41E−02 3′ss CLL 91448953-91449151 91448953-91449074 TGACCCAGGAGG TGACCCAGGCTG ACCCCCGGCGGC GATCAAGACCTT GCTT (745) TGAC (746) 445 chr1: chr1: TTGGAAGCGAAT TTGGAAGCGAAT 1 8 2.17 4.59E−02 3′ss CLL 23398690-23399766 23398690-23399784 CCCCCAAGTCCT CCCCCAAGTGAT TTGTTCTTTTGC GTATATCTCTCA AGTG (210) TCAA (211) 446 chr2: chr2: CCTTTACTTGGG AACCCGGAGAGA 1 8 2.17 4.13E−02 5′ss CLL 64457092-64478252 64456774-64478252 GCTCTCAGCAAC AAAGGGAGCAAC TGATGTTGCCAT TGATGTTGCCAT GCAG (747) GCAG (578) 447 chr14: chr14: GTGGGGGGCCAT GTGGGGGGCCAT 16 75 2.16 9.79E−09 3′ss CLL 23237380-23238985 23237380-23238999 TGCTGCATTTTG TGCTGCATGTAC TATTTTCCAGGT AGTCTTTGCCCG ACAG (122) CTGC (123) 448 chr15: chr15: ACTCAGATGCCG ACTCAGATGCCG 14 65 2.14 1.32E−05 3′ss CLL 74326871-74327483 74326871-74327512 AAAACTCGCCCT AAAACTCGTGCA CAGTCTGAGGTT TGGAGCCCATGG CTGT (748) AGAC (749) 449 chr10: chr10: GCCTACTCTTAA TCATCTTGAAAA 7 34 2.13 4.92E−03 exon CLL 89516679-89519457 89516679-89527429 CCATTAGGGTGG ATGAAAATGTGG incl. ATAGGCATGTAG ATAGGCATGTAG ACCT (750) ACCT (507) 450 chr20: chr20: TGGAGTGCGGAT TGGAGTGCGGAT 2 12 2.12 4.37E−03 3′ss CLL 33703761-33706400 33703736-33706400 TTGCAACACTTG TTGCAACAATCA CTTCCTTCTCCC AAGATCTGCGAG ACAT (751) ACCA (752) 451 chr12: chr12: CAACTGGAGTTC CAACTGGAGTTC 12 53 2.05 3.67E−06 3′ss CLL 105514375-105514866 105514375-105514878 ATTTTCAGGTTT ATTTTCAGACTA TTTGACAGACTA TGTATGAGCACT TGTA (753) TGGG (754) 452 chr1: chr1: CAATGTGTTGAC CAATGTGTTGAC 14 61 2.05 1.87E−03 3′ss CLL 155237988-155238083 155237937-155238083 CATCGCAGTCCC CATCGCAGCCTC CCTACAGCCCTG TCCTGCCAACTT TTCA (755) ACAG (756) 453 chr15: chr15: CAGCTGCTCTCA CAGCTGCTCTCA 16 67 2.00 7.47E−04 3′ss CLL 89870310-89870397 89870294-89870397 GGAGAGAGTGGA GGAGAGAGGTAC CTGGCTCTGTAG AAAGAAGACCCC GTAC (757) TGGC (758) 454 chr3: chr3: TCTCTAGTGGGC TCTCTAGTGGGC 8 35 2.00 7.53E−03 3′ss CLL 141272782-141274647 141272782-141274681 CCTTCTAGTTCT CCTTCTAGGAAT ACAAGGTAAAAC GACCAAAAGAAG TCTA (759) ACAA (760) 455 chr1: chr1: AGCTCCGAGAGG AGCTCCGAGAGG 2 11 2.00 6.28E−03 3′ss CLL 202122978-202123313 202122963-202123313 GCAAGGAGCTCC GCAAGGAGAAAT CTCCCTCCTAGA GTGTCCACTACT AATG (761) GGCC (762) 456 chrX: chrX: GACGTGGCAGCT GACGTGGCAGCT 19 73 1.89 1.20E−04 3′ss CLL 47315813-47326808 47315797-47326808 CATGTGAGCATT CATGTGAGGCTT GTGTCGTTACAG CAGTGTCATTTG GCTT (763) AGGA (764) 457 chr6: chr6: AAGGAAGAACAA AATGTTAAGGAG 2 10 1.87 4.93E−04 exon CLL 25975158-25983391 25973513-25983391 GACTTTGTTTAG TCATCAAGTTAG incl. TGTGACTCTGGA TGTGACTCTGGA TCCA (765) TCCA (766) 458 chr11: chr11: AGGAGAACACCT AGGAGAACACCT 15 55 1.81 1.53E−04 3′ss CLL 10876665-10877690 10876633-10877690 TATTTCAGCTTT TATTTCAGAAAA TATTTTTATGTG GGTGTACCATAC ATAA (767) CTGA (768) 459 chr9: chr9: CTGATGAAAACT CTGATGAAAACT 12 43 1.76 4.16E−05 3′ss CLL 93641235-93648127 93641235-93650030 ACTACAAGACAC ACTACAAGGCCC CTTACAGGCCAG AGACCCATGGAA GAGA (769) AGTG (723) 460 chr8: chr8: GGGGCCACCAGG GGGGCCACCAGG 21 72 1.73 2.11E−05 3′ss CLL 145313817-145314126 145313817-145314142 TTGGCCAGCGGC TTGGCCAGGGCC CCCCTTTCCCAG ATGGCTGAGCAC GGCC (770) GCAG (771) 461 chr7: chr7: TGCACACGCCTC TGCACACGCCTC 4 15 1.68 2.26E−02 3′ss CLL 98579583-98580862 98579583-98580886 TCCTACAGAGTC TCCTACAGGCAG TCTTATGCTGGT CCCAGCAAATCA CCCA (772) TCGA (773) 462 chr22: chr22: GAGCTGGAGAGG GAGCTGGAGAGG 14 46 1.65 2.74E−04 3′ss CLL 50660983-50662569 50661021-50662569 AAGGCGAGAGGC AAGGCGAGGCAG AGCTCGTCGGGA GCACTGGTCGAC GCAG (774) CACT (775) 463 chr6: chr6: GCCCCCGTTTTC GCCCCCGTTTTC 17 55 1.64 1.17E−04 3′ss CLL 31936315-31936399 31936315-31936462 CTGCCCAGCCCT CTGCCCAGTACC TGTCCTCAGTGC TGAAGCTGCGGG ACCC (307) AGCG (308) 464 chr7: chr7: CCGCCTCTGCCT CCGCCTCTGCCT 8 26 1.58 3.53E−03 3′ss CLL 64139714-64150776 64139714-64144464 TCGGATAGGTCT TCGGATAGGAAA GGCCCCACCCTG GGTTGAAAGAGC GAGT (776) CAAC (777) 465 chr12: chr12: TTTCTCATATTG TTTCTCATATTG 5 17 1.58 4.42E−03 3′ss CLL 51174021-51189680 51174021-51189691 CTCAACAGTTCT CTCAACAGGTAT TTTTTAGGTATC CATCTTTATCAG ATCT (778) AAAG (779) 466 chr11: chr11: AGTGGCTTTGGC AGTGGCTTTGGC 15 46 1.55 1.99E−03 intron CLL 126144916-126144918 126144916-126145221 GTCTTATGGAGG GTCTTATGGGAT reten- CTTGCTTGCAGA GGAGGACGAAGG tion GGGG (780) TTGG (781) 467 chr1: chr1: CATAGTGGAAGT CATAGTGGAAGT 20 60 1.54 6.97E−06 3′ss CLL 67890660-67890765 67890642-67890765 GATAGATCTTCT GATAGATCTGGC TTTTCACATTAC CTGAAGCACGAG AGTG (444) GACA (445) 468 chr1: chr1: GGTGACACTCAA GGTGACACTCAA 22 65 1.52 1.10E−05 3′ss CLL 157771381-157771704 157771367-157771704 CTTCACAGGTCT CTTCACAGTGCC CTCCCTCTAGTG TACTGGGGCCAG CCTA (782) AAGC (783) 469 chr2: chr2: GGCAACTTCGTT GGCAACTTCGTT 27 76 1.46 7.08E−07 3′ss CLL 106781255-106782511 106781240-106782511 AATATGAGCTTT AATATGAGGTCT CTACTCAACAGG ATCCAGGAAAAT TCTA (375) GGTG (376) 470 chr14: chr14: CGCTCTCCGCCT AGGGAGACGTTC 19 54 1.46 2.09E−04 exon CLL 75348719-75352288 75349327-75352288 TCCAGAAGGGGT CCTGCCTGGGGT skip CTCCTTATGCCA CTCCTTATGCCA GGGA (208) GGGA (209) 471 chr2: chr2: TTTCCATTGGGC GAGGGCCACCAA 3 10 1.46 4.35E−02 exon CLL 153551136-153571063 153551136-153572508 CAATCAAGATGC TGGGACAAATGC incl. CTGGAATGATGT CTGGAATGATGT CGTC (784) CGTC (785) 472 chrX: chrX: AGAGACAAAGAG AGAGACAAAGAG 33 92 1.45 4.85E−06 3′ss CLL 118759359-118763280 118759342-118763280 AAGAAAAACTCT AAGAAAAATTAA TACTGTTTTACA CTCTGCTGTTTG GTTA (786) CTGC (787) 473 chr17: chr17: CTCACCAGCGCC CTCACCAGCGCC 5 15 1.42 1.43E−03 exon CLL 27238402-27239499 27238255-27239499 ATCGTCAGCTCT ATCGTCAGATGG incl. AGGAGTTCCAGA CAAGGTCAGCCC GCCT (788) CGGC (789) 474 chr12: chr12: ATCAGGTGCTCA ATCAGGTGCTCA 11 30 1.37 9.13E−04 3′ss CLL 50821692-50822699 50821692-50822717 TCCTGAGGTGTC TCCTGAGGGTAA TGTCTTTAATAC TGCAGAGCTCTC AGGT (790) AGAA (791) 475 chr6: chr6: TCTGGCAGCCCA TCTGGCAGCCCA 17 45 1.35 1.98E−04 3′ss CLL 43152643-43153228 43152643-43153193 CGATGCTGCAAG CGATGCTGGGAG ATGGCATCGAGC TCGGGCTCACGT AGCA (792) CCTT (793) 476 chr3: chr3: AGAATTTTAAGA AGAATTTTAAGA 11 29 1.32 1.64E−03 3′ss CLL 3186394-3188099 3186394-3188113 TACTTCAGATTT TACTTCAGGTTT TGTCTTGTAGGT TATGGGAGAATT TTTA (794) GTAG (795) 477 chr7: chr7: CCGCCTCTGCCT CCGCCTCTGCCT 1 4 1.32 2.43E−02 3′ss CLL 64139714-64150765 64139714-64144464 TCGGATAGGCTT TCGGATAGGAAA TATTTAGGTCTG GGTTGAAAGAGC GCCC (796) CAAC (777) 478 chr3: chr3: GAGCTAGTCAGA AAATTCTTGACC 15 38 1.29 1.66E−02 exon CLL 56606456-56626997 56605330-56626997 CTTTAGAGGAAA AATCTAGGGAAA incl. CAGTACTGCTGG CAGTACTGCTGG AGCA (797) AGCA (798) 479 chr22: chr22: CTTCATCTGTGG CTTCATCTGTGG 25 61 1.25 5.02E−06 3′ss CLL 24043032-24047615 24037704-24047615 ATAAGCAGGTCA ATAAGCAGTGCA TGTCCTCCAGGT GGCCAAGGCCCC TTCT (799) CTGC (800) 480 chr17: chr17: CCGGAGCCCCTT CCGGAGCCCCTT 8 20 1.22 1.07E−02 3′ss CLL 45229302-45232037 45229284-45232037 CAAAAAAGACTT CAAAAAAGTCTG TTCGTGTTTTAC TTGCCAGAATCG AGTC (327) GCCA (328) 481 chr1: chr1: AGTATGGGATAT TCATTCTTATTT 8 20 1.22 2.03E−02 exon CLL 62149218-62152463 62149218-62160368 TTTAAAAGATTG CAATGCAGATTG incl. TTGGACCTTCAG TTGGACCTTCAG ATGG (801) ATGG (802) 482 chr22: chr22: CTTTATCTGTGC CTTCATCTGTGG 31 73 1.21 1.26E−05 exon CLL 24037704-24042912 24037704-24047615 ATGAACAGTGCA ATAAGCAGTGCA incl. GGCCAAGGCCCC GGCCAAGGCCCC CTGC (803) CTGC (800) 483 chr7: chr7: AAGTCGTCCTCT AGAGAGAAACAT 18 42 1.18 2.78E−02 exon CLL 104844232-104909252 104844232-105029094 TCAGAAAGGCCG CCGAAAAAGCCG incl. GAGCCTCAACAG GAGCCTCAACAG AAAG (804) AAAG (805) 484 chr2: chr2: TGGGCTACCTTA TGGGCTACCTTA 23 53 1.17 3.28E−02 exon CLL 85779690-85780061 85779104-85780061 ACCCTGGGGTAT ACCCTGGGGATT incl. TTACACAGAGTC TTTGACCCTCGT GGCG (806) GTGG (807) 485 chr1: chr1: GACTGCCCTAAA GACTGCCCTAAA 10 23 1.13 4.92E−03 3′ss CLL 52902647-52903891 52902635-52903891 AGGAAAAGTTTA AGGAAAAGACTA CTGTTTAGACTA AAGAAGAAAGAC AAGA (808) AGTG (809) 486 chr3: chr3: TGATAGTTGGAG TGATAGTTGGAG 11 25 1.12 3.47E−03 3′ss CLL 179065598-179066635 179065598-179066632 CGGAGACTCATA CGGAGACTTAGC ATGGCAGAACCT ATAATGGCAGAA GTTT (810) CCTG (811) 487 chr1: chr1: TCATTCTTATTT TCATTCTTATTT 5 12 1.12 3.19E−02 exon CLL 62152593-62160368 62149218-62160368 CAATGCAGAGAC CAATGCAGATTG incl. AGGGTCTTGCTC TTGGACCTTCAG TGTT (812) ATGG (802) 488 chr19: chr19: TGACGGTGCCAC TGACGGTGCCAC 30 65 1.09 4.13E−02 exon CLL 53935281-53936832 53935281-53945048 CGCGGCGCTTTT CGCGGCGCAGAG incl. CTCCCTTAGATG GAGTCTGCAATG CCTT (813) CCGA (814) 489 chr19: chr19: GCAGTGGCTGGA GCAGTGGCTGGA 42 85 1.00 4.02E−05 3′ss CLL 19414656-19416657 19414721-19416657 GATCAAAGTTTC GATCAAAGAGAG ACCCCCAGAGGG AGTGTGCCTATT AGCC (815) GACT (816) 490 chrX: chrX: GGACGATGGGGA GGACGATGGGGA 3 7 1.00 8.68E−03 3′ss CLL 47103949-47104083 47103949-47104080 TGAGAAAGATGA TGAGAAAGAAGA CGAGGAGGATAA TGACGAGGAGGA AGAT (817) TAAA (818) 491 chr5: chr5: ACTCTTATGCAG ACTCTTATGCAG 24 48 0.97 7.63E−03 3′ss CLL 1579599-1585098 1581810-1585098 TCCCCATGGACT TCCCCATGAGGA GAACCATCAAGA GATCCTAGTCTC CACC (819) ACCA (531) 492 chr17: chr17: GACCCATGCATC GACCCATGCATC 47 93 0.97 2.22E−02 3′ss CLL 73587327-73587681 73587327-73587696 CTCCTGTGCTCC CTCCTGTGTGGG TCCCACTGCAGT CACAGTGGCTCA GGGC (820) GGGA (821) 493 chr18: chr18: CCAAGTTTTGTG CCAAGTTTTGTG 38 75 0.96 7.90E−03 3′ss CLL 224200-224923 224179-224923 AAAGAAAGTGTA AAAGAAAGAACA TGTTTTGTTCAC TCAGATACCAAA GACA (116) CCTA (117) 494 chr16: chr16: CATCAAGCAGCT CATCAAGCAGCT 10 20 0.93 2.86E−02 3′ss CLL 57473207-57474683 57473246-57474683 GTTGCAATGTTT GTTGCAATCTGC AGTCCCAGGAAG CCACAAAGAATC CACC (822) CAGC (823) 495 chr7: chr7: TGAGAGTCTTCA TGAGAGTCTTCA 45 86 0.92 7.69E−08 3′ss CLL 99943591-99947339 99943591-99947421 GTTACTAGTTTG GTTACTAGAGGC TCTTTCCTAGAT GGATTTCCCTGA CCAG (420) CTGA (421) 496 chr12: chr12: CAATCATTGACA CAATCATTGACA 29 54 0.87 3.27E−02 3′ss CLL 47599928-47600293 47599852-47600293 ATATTATGACCC ATATTATGGAAC TGCATGTGATGG TGACTCAGCGCA ATCA (824) AGAA (825) 497 chr9: chr9: GGGACACTGTGC GGGACACTGTGC 43 72 0.73 1.74E−02 3′ss CLL 140633231-140637822 140633231-140637843 CGAATGAACTTG CGAATGAACAGC CTTGCCTTTTGT TGCAGTATCTCG TTTA (826) GAAG (827) 498 chr19: chr19: TCAGGGGGCGCG TCGAGCCAGGCT 10 17 0.71 2.37E−02 exon CLL 17654242-17657494 17654440-17657494 TGCTGAAGGAGC GCAAAAAGGAGC skip TGCCTGAGTTCG TGCCTGAGTTCG AGGG (828) AGGG (829) 499 chr6: chr6: CTACAACCAGAG CTACAACCAGAG 57 92 0.68 2.50E−03 3′ss CLL 29691704-29691949 29691704-29691966 CGAGGCTGGGTC CGAGGCTGGGAA TCACACCCTCCA TGAATGGCTGCG GGGA (830) ACAT (831) 500 chr20: chr20: TGCCTAAGGCGG TGCCTAAGGCGG 54 87 0.68 4.59E−02 3′ss CLL 30310151-30310420 30310133-30310420 ATTTGAATCTCT ATTTGAATAATC TTCTCTCCCTTC TTATCTTGGCTT AGAA (479) TGGA (480) 501 chr4: chr4: TCCAACAAGCAC TCCAACAAGCAC 55 87 0.65 1.64E−04 3′ss CLL 17806394-17806729 17806379-17806729 CTCTGAAGTCTT CTCTGAAGGTTA CTCATTCACAGG AGGCTACCTTTC TTAA (832) CAGA (833) 502 chr9: chr9: CACCACAAAATC CACCACAAAATC 41 65 0.65 4.07E−03 3′ss CLL 140622981-140637822 140622981-140637843 ACAGACAGCTTG ACAGACAGCAGC CTTGCCTTTTGT TGCAGTATCTCG TTTA (458) GAAG (459) 503 chr1: chr1: GAATCCGTATCT GAATCCGTATCT 45 70 0.63 4.59E−02 3′ss CLL 155278756-155279833 155278756-155279854 GGGAACAGAGCC GGGAACAGAATG CTTTGCTCCTCC AACGGAGACCAG CTCA (432) AATT (433) 504 chr17: chr17: GTTCCCGAGGCT GTTCCCGAGGCT 60 90 0.58 8.49E−05 3′ss CLL 40690773-40692967 40690773-40695045 GTCACCAGGGTG GTCACCAGTGGA TTCCCTCAGGTC TACTGAGGCTGT AATG (834) GTGG (835) 505 chr12: chr12: ATTTCCAGAGGA ATTTCCAGAGGA 51 76 0.57 1.45E−05 3′ss CLL 95660408-95663814 95660408-95663826 TTTACACTTTTG TTTACACTGGTC CTTGACAGGGTC AGTGCTGCTTGC AGTG (462) CCAT (463) 506 chr3: chr3: CCAGATCAACAC CCAGATCAACAC 44 65 0.55 2.77E−02 3′ss CLL 133371473-133372188 133371458-133372188 AATTGATAGTCG AATTGATAATGT TACTCTTTCAGA CAGCAATATTTC TGTC (836) CAAC (837) 507 chr19: chr19: CGTCCTGCCCCC CGTCCTGCCCCC 67 94 0.48 2.30E−02 3′ss CLL 7075116-7075665 7075116-7075686 AACTGCCGCTCT AACTGCCGCCTC GTCTTCCCTGTT TCAGCGAGAAGG CCCA (838) ACAC (839) 508 chr10: chr10: TGACGTTCTCTG TGACGTTCTCTG 53 74 0.47 2.22E−03 3′ss CLL 75554088-75554298 75554088-75554313 TGCTCCAGTGGT TGCTCCAGGTTC TTCTCCCACAGG CCGGCCCCCAAG TTCC (466) TCGC (467) 509 chr19: chr19: TGCAGGGGGAGC TGCAGGGGGAGC 48 66 0.45 6.62E−03 3′ss CLL 11558433-11558507 11558433-11558537 AGCCCAAGGAGG AGCCCAAGCCGG CCCCACCGCCAC CCAGCCCTGCTG TGTC (840) AGGA (841) 510 chr1: chr1: GACTGCCCTAAA GACTGCCCTAAA 55 74 0.42 8.74E−03 3′ss CLL 52902650-52903891 52902635-52903891 AGGAAAAGCAGT AGGAAAAGACTA TTACTGTTTAGA AAGAAGAAAGAC CTAA (842) AGTG (809) 511 chr17: chr17: CTATGAGGCCAT GTTCCCGAGGCT 68 87 0.35 1.45E−03 exon CLL 40693224-40695045 40690773-40695045 GACTGCAGTGGA GTCACCAGTGGA incl. TACTGAGGCTGT TACTGAGGCTGT GTGG (843) GTGG (835) 512 chr5: chr5: CTTCTCAAGATC CTTCTCAAGATC 70 86 0.29 2.73E−02 3′ss CLL 139865317-139866542 139865317-139866590 AGTCTCAGGTGC AGTCTCAGGAAC CACGTGTGCCAA CTGACAGAACTT CGCA (844) CACA (845) 513 chr6: chr6: ACCTTAACAAGA AATCACTAGGAA 58 71 0.29 1.38E−02 exon CLL 127636041-127637594 127636041-127648146 TTTATGAGACTT CTCCAGAGACTT incl. CCTTTAATAAGT CCTTTAATAAGT GTTG (846) GTTG (847) 514 chr4: chr4: ACTGGGCTTCCA ACTGGGCTTCCA 60 72 0.26 4.54E−02 exon CLL 54266006-54280781 54266006-54292038 CCGAGCAGAAAC CCGAGCAGGAGA incl. AGCACTTCTTCT TTACCTGGGGCA CAGT (848) ATTG (849) 515 chr9: chr9: CTGAAGACGGGA CTGAAGACGGGA 87 92 0.08 2.80E−02 3′ss CLL 130566979-130569251 130566979-130569270 TTCTTTAGCTCT TTCTTTAGGTTC CCCCACCTGGTG GGGAGCGGATCC CAGG (850) GCAT (851) 516 chr17: chr17: ATCTCAGGAGCA CCCACCCCTTCA 93 98 0.07 4.18E−03 5′ss CLL 72759659-72763074 72760785-72763074 CCTGAATGGTCC CCCTGCAGGTCC CCTGCCTGTGCC CCTGCCTGTGCC CTTC (852) CTTC (853) 517 chr2: chr2: AGCAAGTAGAAG AGCAAGTAGAAG 0 72 6.19 1.51E−10 3′ss Mel. 109102364-109102954 109102364-109102966 TCTATAAAATTT TCTATAAAATAC ACCCCCAGATAC AGCTGGCTGAAA AGCT (1) TAAC (2) 518 chr19: chr19: GGCCCTTTTGTC GGCCCTTTTGTC 0 72 6.19 7.67E−09 3′ss Mel. 57908542-57909780 57908542-57909797 CTCACTAGCATT CTCACTAGGTTC TCTGTTCTGACA TTGGCATGGAGC GGTT (7) TGAG (8) 519 chr2: chr2: TGACCACGGAGT TGACCACGGAGT 0 59 5.91 1.12E−08 3′ss Mel. 232196609-232209660 232196609-232209686 ACCTGGGGCCCT ACCTGGGGATCA TTTTTCTCTTTC TGACCAACACGG CTTC (37) GGAA (38) 520 chr1: chr1: CAAGTATATGAC CAAGTATATGAC 0 56 5.83 3.98E−05 3′ss Mel. 245246990-245288006 245246990-245250546 TGAAGAAGATCC TGAAGAAGGTGA TGAATTCCAGCA GCCTTTTTCTCA AAAC (21) AGAG (22) 521 chr11: chr11: GGCCACACGCCT GGCCACACGCCT 0 54 5.78 1.58E−06 3′ss Mel. 65635911-65635980 65635892-65635980 CTGCCAAGCCCC CTGCCAAGACAT TCTCCCCTGGCA TGATGAGTGTGA CAGA (854) GTCT (855) 522 chr3: chr3: TGCAGTTTGGTC TGCAGTTTGGTC 0 49 5.64 5.19E−07 3′ss Mel. 9960293-9962150 9960293-9962174 AGTCTGTGCCTT AGTCTGTGGGCT CCTCACCCCTCT CTGTGGTATATG CCTC (23) ACTG (24) 523 chr3: chr3: GAGTACGAGGTC GAGTACGAGGTC 0 48 5.61 2.52E−15 3′ss Mel. 48457878-48459319 48457860-48459319 TCCAGCAGCCTG TCCAGCAGCCTC CCCTGTGCCTAC GTGTGCATCACC AGCC (856) GGGG (857) 524 chr10: chr10: TACCTCTGGTTC TACCTCTGGTTC 0 47 5.58 5.54E−06 3′ss Mel. 99214556-99215395 99214556-99215416 CTGTGCAGTCTT CTGTGCAGTTCT CGCCCCTCTTTT GTGGCACTTGCC CTTA (13) CTGG (14) 525 chr1: chr1: TCTTTGGAAAAT TCTTTGGAAAAT 0 45 5.52 3.06E−06 3′ss Mel. 101458310-101460665 101458296-101460665 CTAATCAATTTT CTAATCAAGGGA CTGCCTATAGGG AGGAAGATCTAT GAAG (25) GAAC (26) 526 chr9: chr9: AGCGCATCGCAG AGCGCATCGCAG 0 45 5.52 1.42E−03 3′ss Mel. 90582559-90584108 90582574-90584108 CTTCCAAGTACT CTTCCAAGGCTC TCTTCACAGCTC TCCTCCATCAGT CCCT (858) ACTT (859) 527 chr1: chr1: TCACTCAAACAG TCACTCAAACAG 0 44 5.49 1.90E−07 3′ss Mel. 179835004-179846373 179834989-179846373 TAAACGAGTTTT TAAACGAGGTAT ATCATTTACAGG GTGACGCATTCC TATG (53) CAGA (54) 528 chr14: chr14: AGTTAGAATCCA AGTTAGAATCCA 0 41 5.39 4.30E−08 3′ss Mel. 74358911-74360478 74358911-74360499 AACCAGAGTGTT AACCAGAGCTCC GTCTTTTCTCCC TGGTACAGTTTG CCCA (61) TTCA (62) 529 chr11: chr11: TGGGCAGCCCCC TGGGCAGCCCCC 0 39 5.32 2.61E−02 3′ss Mel. 117167925-117186250 117167677-117186250 CGCAGACGTTGG CGCAGACGCTCA TTTTTCAGCAGA ACATCCTGGTGG CCTG (860) ATAC (861) 530 chr20: chr20: AGAACTGCACCT AGAACTGCACCT 0 36 5.21 6.58E−07 3′ss Mel. 62701988-62703210 62701988-62703222 ACACACAGCCCT ACACACAGGTGC GTTCACAGGTGC AGACCCGCAGCT AGAC (29) CTGA (30) 531 chr18: chr18: AGAAAGAGCATA AGAAAGAGCATA 0 33 5.09 6.82E−09 3′ss Mel. 33605641-33606862 33573263-33606862 AATTGGAAATAT AATTGGAAGAGT TGGACATGGGCG ACAAGCGCAAGC TATC (91) TAGC (92) 532 chr3: chr3: AACCAAGAGGAC AACCAAGAGGAC 0 32 5.04 1.83E−02 3′ss Mel. 52283338-52283671 52283338-52283685 CCACACAGGATG CCACACAGGTTC GTCTTCACAGGT TCAAAGCTGGCC TCTC (862) CAGA (863) 533 chr9: chr9: AAATGAAGAAAC AAATGAAGAAAC 0 32 5.04 6.82E−09 3′ss Mel. 125759640-125760854 125759640-125760875 TCCTAAAGCCTC TCCTAAAGATAA TCTCTTTCTTTG AGTCCTGTTTAT TTTA (67) GACC (68) 534 chr12: chr12: AATATTGCTTTA AATATTGCTTTA 0 31 5.00 9.14E−06 3′ss Mel. 116413154-116413319 116413118-116413319 CCAAACAGGGAC CCAAACAGGTCA CCCTTCCCCTTC CGGAGGAGTAAA CCCA (77) GTAT (78) 535 chr18: chr18: TTGGACCGGAAA TTGGACCGGAAA 1 62 4.98 1.13E−06 3′ss Mel. 683395-685920 683380-685920 AGACTTTGAGTC AGACTTTGATGA TCTTTTTGCAGA TGGATGCCAACC TGAT (15) AGCG (16) 536 chr1: chr1: ATCAGAAATTCG ATCAGAAATTCG 0 29 4.91 8.06E−03 3′ss Mel. 212515622-212519131 212515622-212519144 TACAACAGGTTT TACAACAGCTCC CTTTTAAAGCTC TGGAGCTTTTTG CTGG (65) ATAG (66) 537 chr1: chr1: CTCAGAGCCAGG CTCAGAGCCAGG 0 29 4.91 3.06E−05 3′ss Mel. 35871069-35873587 35871069-35873608 CTGTAGAGATGT CTGTAGAGTCCG TTTCTACCTTTC CTCTATCAAGCT CACA (105) GAAG (106) 538 chrX: chrX: GTCTTGAGAATT ACTTCCTTAGTG 0 29 4.91 1.16E−06 5′ss Mel. 47059943-47060292 47059013-47060292 GGAAGCAGGTGG GTTTCCAGGTGG TGGTGCTCACCA TGGTGCTCACCA ACAC (113) ACAC (112) 539 chr2: chr2: AAATTTAACATT AAATTTAACATT 0 28 4.86 3.75E−06 3′ss Mel. 24207701-24222524 24207701-24222541 ACTCATAGTTTT ACTCATAGAGTA TGCTGTTTTACA AGCCATATCAAA GAGT (546) GACT (547) 540 chr5: chr5: CTCCATGCTCAG CTCCATGCTCAG 0 28 4.86 8.03E−04 3′ss Mel. 869519-870587 865696-870587 CTCTCTGGTTTC CTCTCTGGGGAA TTTCAGGGCCTG GGTGAAGAAGGA CCAT (128) GCTG (129) 541 chr20: chr20: ACATGAAGGTGG ACATGAAGGTGG 0 27 4.81 4.86E−06 3′ss Mel. 34144042-34144725 34144042-34144743 ACGGAGAGGCTC ACGGAGAGGTAC CCCTCCCACCCC TGAGGACAAATC AGGT (49) AGTT (50) 542 chr2: chr2: TGGGAGGAGCAT TGGGAGGAGCAT 0 27 4.81 1.72E−04 3′ss Mel. 97285513-97297048 97285499-97297048 GTCAACAGAGTT GTCAACAGGACT TCCCTTATAGGA GGCTGGACAATG CTGG (9) GCCC (10) 543 chr19: chr19: AGCCATTTATTT AGCCATTTATTT 1 54 4.78 1.18E−09 3′ss Mel. 9728842-9730107 9728855-9730107 GTCCCGTGGGAA GTCCCGTGGGTT CCAATCTGCCCT TTTTTCCAGGGA TTTG (160) ACCA (161) 544 chr15: chr15: ATATTCCTTTTA ATATTCCTTTTA 0 25 4.70 3.65E−06 3′ss Mel. 49420970-49421673 49420957-49421673 TTTCTAAGTCTT TTTCTAAGGAGT TTGTCTTAGGAG TAAACATAGATG TTAA (864) TAGC (865) 545 chr12: chr12: ATTTGGACTCGC ATTTGGACTCGC 1 49 4.64 6.42E−06 3′ss Mel. 105601825-105601935 105601807-105601935 TAGCAATGATGT TAGCAATGAGCA CTGTTTATTTTT TGACCTCTCAAT AGAG (41) GGCA (42) 546 chr14: chr14: AGATGTCAGGTG AGATGTCAGGTG 0 24 4.64 2.35E−03 3′ss Mel. 75356052-75356580 75356052-75356599 GGAGAAAGCCTT GGAGAAAGCTGT TGATTGTCTTTT TGGAGACACAGT CAGC (89) TGCA (90) 547 chr11: chr11: CATAAAATTCTA CATAAAATTCTA 0 23 4.58 4.56E−05 3′ss Mel. 4104212-4104471 4104212-4104492 ACAGCTAATTCT ACAGCTAAGCAA CTTTCCTCTGTC GCACTGAGCGAG TTCA (69) GTGA (70) 548 chr15: chr15: GAAACCAACTAA GAAACCAACTAA 0 23 4.58 2.75E−04 3′ss Mel. 59209219-59224554 59209198-59224554 AGGCAAAGCCCA AGGCAAAGGTAA TTTTCCTTCTTT AAAACATGAAGC CGCA (101) AGAT (102) 549 chr22: chr22: CTGGGAGGTGGC CTGGGAGGTGGC 0 23 4.58 1.03E−06 3′ss Mel. 19044699-19050714 19044675-19050714 ATTCAAAGCCCC ATTCAAAGGCTC ACCTTTTGTCTC TTCAGAGGTGTT CCCA (45) CCTG (46) 550 chr3: chr3: CACTGCTGGGAG CACTGCTGGGAG 0 23 4.58 5.29E−10 3′ss Mel. 129284872-129285369 129284860-129285369 AGTGGAAGTTGC AGTGGAAGATTC TTCCACAGATTC CTGAGAGCTGCC CTGA (524) GGCC (525) 551 chr9: chr9: GGTCCTGAACGC GGTCCTGAACGC 0 23 4.58 1.89E−04 3′ss Mel. 138903859-138905044 138903870-138905044 TGTGAAATAACT TGTGAAATTGTA TCGCCCCCAGCT CTGTCAGAACTT TCAA (866) CGCC (867) 552 chr6: chr6: TGGAGCAGTATG TGGAGCAGTATG 0 22 4.52 8.93E−03 3′ss Mel. 35255622-35258029 35255622-35258042 CCAGCAAGACTT CCAGCAAGGTTC TTCCCCCAGGTT TTCATGACAGCC CTTC (868) AGAT (869) 553 chr8: chr8: TCGTGCAGACCC TCGTGCAGACCC 0 22 4.52 3.21E−11 3′ss Mel. 28625893-28627405 28625839-28627405 TGGAGAAGATCT TGGAGAAGCATG CACAGATGTGCA GCTTCAGTGATA GTCT (870) TTAA (871) 554 chr6: chr6: CCGGGGCCTTCG CCGGGGCCTTCG 2 67 4.50 2.74E−12 3′ss Mel. 10723474-10724788 10723474-10724802 TGAGACCGCTTG TGAGACCGGTGC TTTTCTGCAGGT AGGCCTGGGGTA GCAG (95) GTCT (96) 555 chr4: chr4: GTGCCAACGAGG GTGCCAACGAGG 2 65 4.46 9.90E−07 3′ss Mel. 184577127-184580081 184577114-184580081 ACCAGGAGTTCT ACCAGGAGATGG TTATTTCAGATG AACTAGAAGCAT GAAC (734) TACG (735) 556 chr22: chr22: CTCTCTCCAACC CTCTCTCCAACC 0 21 4.46 4.84E−04 3′ss Mel. 39064137-39066874 39064137-39066888 TGCATTCTCATC TGCATTCTTTGG TCGCCCACAGTT ATCGATCAACCC GGAT (140) GGGA (141) 557 chr9: chr9: TTGAAGCTCAGT TTGAAGCTCAGT 0 21 4.46 3.30E−03 3′ss Mel. 37501841-37503015 37501841-37503039 GAGAAAAGTTCT GAGAAAAGGATG TCTGTTTATGTC ATGGAGATAGCC TTCC (872) AAAG (873) 558 chr14: chr14: CAGTTATAAACT CAGTTATAAACT 0 20 4.39 2.55E−03 3′ss Mel. 71059726-71060012 71059705-71060012 CTAGAGTGAGTT CTAGAGTGCTTA TATTTTCCTTTT CTGCAGTGCATG ACAA (79) GTAT (80) 559 chr17: chr17: GGAGCAGTGCAG GGAGCAGTGCAG 0 20 4.39 2.74E−12 3′ss Mel. 71198039-71199162 71198039-71199138 TTGTGAAATCAT TTGTGAAAGTTT TACTTCTAGATG TGATTCATGGAT ATGC (31) TCAC (32) 560 chr9: chr9: CGCCCTGACACA CGCCCTGACACA 0 20 4.39 1.26E−04 3′ss Mel. 35608506-35608842 35608506-35608858 CAATCAGGACTT CAATCAGGGCTC CTCTATCTACAG TGTTGCAAGAGG GCTC (874) GGGT (875) 561 chrX: chrX: ACTTCCTTAGTG ACTTCCTTAGTG 0 20 4.39 2.32E−03 3′ss Mel. 47059013-47059808 47059013-47060292 GTTTCCAGGTTG GTTTCCAGGTGG CCAGGGCACTGC TGGTGCTCACCA AGCT (111) ACAC (112) 562 chr12: chr12: CTTGGAGCTGAC CTTGGAGCTGAC 4 96 4.28 5.10E−13 3′ss Mel. 107378993-107380746 107379003-107380746 GCCGACGGGGAA GCCGACGGTTTA CTGACAAGATCA TTGCAGGGAACT CATT (130) GACA (131) 563 chr10: chr10: TTGCTGGCCATC TTGCTGGCCATC 0 18 4.25 1.13E−14 3′ss Mel. 133782836-133784141 133782073-133784141 GGATTGGGCCCT GGATTGGGGATC TCGTTTCAGGAT TATATTGGAAGG GGAT (876) CGTC (877) 564 chr11: chr11: CCACCGCCATCG CCACCGCCATCG 0 18 4.25 6.04E−04 3′ss Mel. 64877395-64877934 64877395-64877953 ACGTGCAGTACC ACGTGCAGGTGG TCTTTTTACCAC GGCTCCTGTACG CAGG (167) AAGA (168) 565 chr21: chr21: ATCATAGCCCAC ATCATAGCCCAC 1 35 4.17 1.72E−04 3′ss Mel. 37416267-37417879 37416254-37417879 ATGTCCAGTTTT ATGTCCAGGTAA TCTTTCTAGGTA AAGCAGCGTTTA AAAG (695) ATGA (696) 566 chr15: chr15: TGATTCCAAGCA TGATTCCAAGCA 1 34 4.13 1.03E−06 3′ss Mel. 25213229-25219533 25213229-25219457 AAAACCAGCCTT AAAACCAGGCTC CCCCTAGGTCTT CATCTACTCTTT CAGA (230) GAAG (231) 567 chr17: chr17: TACTGAAATGTG TACTGAAATGTG 0 16 4.09 5.46E−04 3′ss Mel. 34942628-34943454 34942628-34943426 ATGAACATATCC ATGAACATATCC AGGTAATCGAGA AGAAGCTTGGAA GACC (124) GCTG (125) 568 chr2: chr2: CCATTCGAGAGC CCATTCGAGAGC 0 16 4.09 2.25E−03 3′ss Mel. 219610954-219611752 219610954-219611725 ATCAGAAGATTG ATCAGAAGCTAA GGAGGAAGGACC ACCATTTCCCAG GGCT (878) GCTC (879) 569 chr10: chr10: TCTTGCCAGAGC TCTTGCCAGAGC 0 15 4.00 9.94E−07 3′ss Mel. 99219232-99219415 99219283-99219415 TGCCCACGCTCT TGCCCACGCTTC CCACCCTCAGCT TTTCCTTGCTGC GCCT (587) TGGA (588) 570 chr11: chr11: AGATCGCCTGGC AGATCGCCTGGC 0 15 4.00 9.65E−05 3′ss Mel. 3697619-3697738 3697606-3697738 TCAGTCAGTTTT TCAGTCAGACAT TCTCTCTAGACA GGCCAAACGTGT TGGC (187) AGCC (188) 571 chr11: chr11: CGGCGCGGGCAA CGGCGCGGGCAA 0 15 4.00 4.00E−05 3′ss Mel. 62648919-62649352 62648919-62649364 CCTGGCGGCCCC CCTGGCGGGTCT CATTTCAGGTCT GAAGGGGCGTCT GAAG (165) CGAT (166) 572 chr1: chr1: TCAGGAGCAGAG CTCAGGGAAGGG 0 15 4.00 2.96E−02 5′ss Mel. 113195986-113196219 113192091-113196219 AGGAAAAGTGCA GCAGCACATGCA TTTGCCCAGTAT TTTGCCCAGTAT AACA (880) AACA (881) 573 chr1: chr1: CGATCTCCCAAA CGATCTCCCAAA 0 15 4.00 5.55E−03 3′ss Mel. 52880319-52880412 52880319-52880433 AGGAGAAGTCTG AGGAGAAGCCCC ACCAGTCTTTTC TCCCCTCGCCGA TACA (55) GAAA (56) 574 chr15: chr15: TCACACAGGATA GCCTCACTGAGC 1 30 3.95 6.03E−06 exon Mel. 25212299-25213078 25207356-25213078 ATTTGAAAGTGT AACCAAGAGTGT incl. CAGTTGTACCCG CAGTTGTACCCG AGGC (164) AGGC (145) 575 chr11: chr11: TGCAGCTGGCCC TGCAGCTGGCCC 0 14 3.91 1.39E−07 3′ss Mel. 64002365-64002911 64002365-64002929 CCGCCCAGGTCT CCGCCCAGGCCC TTTCTCTCCCAC CTGTCTCCCAGC AGGC (638) CTGA (639) 576 chr12: chr12: GCCTGCCTTTGA GCCTGCCTTTGA 0 14 3.91 1.83E−03 3′ss Mel. 113346629-113348840 113346629-113348855 TGCCCTGGATTT TGCCCTGGGTCA TGCCCGAACAGG GTTGACTGGCGG TCAG (71) CTAT (72) 577 chr17: chr17: CCAAGCTGGTGT CCAAGCTGGTGT 0 14 3.91 1.08E−03 3′ss Mel. 78188582-78188831 78188564-78188831 GCGCACAGGCCT GCGCACAGGCAT CTCTTCCCGCCC CATCGGGAAGAA AGGC (73) GCAC (74) 578 chr2: chr2: GTGTGGCAAGTA GTGTGGCAAGTA 0 14 3.91 1.45E−02 3′ss Mel. 85848702-85850728 85848702-85850768 CTTTCAAGTATC CTTTCAAGGCCG TGCCCTTCTATT GGGTTTGAAGTC ACAG (882) TCAC (883) 579 chr12: chr12: AAAATCATTGAT AAAATCATTGAT 0 13 3.81 1.44E−03 3′ss Mel. 29450133-29460566 29450133-29460590 TCCCTTGAAATT TCCCTTGAGTGG CTCTTTACTCTA TTAGACGATGCT CCTT (884) ATTA (885) 580 chr14: chr14: GTGGGGGGCCAT GTGGGGGGCCAT 0 13 3.81 2.75E−04 3′ss Mel. 23237380-23238985 23237380-23238999 TGCTGCATTTTG TGCTGCATGTAC TATTTTCCAGGT AGTCTTTGCCCG ACAG (122) CTGC (123) 581 chr22: chr22: CGCTGGCACCAT CGCTGGCACCAT 0 13 3.81 5.09E−08 3′ss Mel. 36627480-36629198 36627512-36629198 GAACCCAGTATT GAACCCAGAGAG TCCAGGACCAAG CAGTATCTTTAT TGAG (199) TGAG (200) 582 chr19: chr19: TGCCTGTGGACA TGCCTGTGGACA 0 12 3.70 4.53E−04 3′ss Mel. 14031735-14034130 14031735-14034145 TCACCAAGCCTC TCACCAAGGTGC GTCCTCCCCAGG CGCCTGCCCCTG TGCC (59) TCAA (60) 583 chr20: chr20: TTTGCAGGGAAT TTTGCAGGGAAT 0 12 3.70 9.65E−05 3′ss Mel. 35282126-35284762 35282104-35284762 GGGCTACATCCC GGGCTACATACC CTTGGTTCTCTG ATCTGCCAGCAT TTAC (35) GACT (36) 584 chr22: chr22: TGCTCAGAGGTG TGCTCAGAGGTG 0 12 3.70 8.43E−07 3′ss Mel. 19948812-19950181 19948812-19950049 CTTTGAAGCCCA CTTTGAAGATGC TCCACAACCTGC CGGAGGCCCCGC TCAT (886) CTCT (887) 585 chr2: chr2: CAAGATAGATAT CAAGATAGATAT 0 12 3.70 3.94E−03 3′ss Mel. 170669034-170671986 170669016-170671986 TATAGCAGGTGG TATAGCAGAACT CTTTTGTTTTAC TCGATATGACCT AGAA (99) GCCA (100) 586 chr15: chr15: GCCTCACTGAGC GCCTCACTGAGC 2 37 3.66 8.44E−08 exon Mel. 25207356-25212175 25207356-25213078 AACCAAGAGTAG AACCAAGAGTGT incl. TGACTTGTCAGG CAGTTGTACCCG AGGA (144) AGGC (145) 587 chr11: chr11: CCACGGCCACGG CCACGGCCACGG 4 60 3.61 3.80E−03 3′ss Mel. 8704812-8705536 8704812-8705552 CCGCATAGCTTT CCGCATAGGCAA GTATTCCTGCAG GCACCGGAAGCA GCAA (888) CCCC (889) 588 chr11: chr11: CATGCCGGGGCC CATGCCGGGGCC 0 11 3.58 1.83E−02 3′ss Mel. 11988666-11989941 11988645-11989941 AGAGGATGGCTC AGAGGATGCTCT TTTCCACCTGTC GCACCCGGGACA TGCA (890) GTGA (891) 589 chr16: chr16: GGCCAAGCAAGA GGCCAAGCAAGA 0 11 3.58 1.88E−02 3′ss Mel. 19838459-19843229 19838459-19867808 ACAAAAAGTATT ACAAAAAGTGAA TTCTTCTAGGAT ATGCAAAATGGA GGAA (892) GGAC (893) 590 chr1: chr1: GGCTCCCATTCT GGCTCCCATTCT 0 11 3.58 2.42E−03 3′ss Mel. 155630724-155631097 155630704-155631097 GGTTAAAGAGTG GGTTAAAGGCCA TTCTCATTTCCA GTCTGCCATCCA ATAG (195) TCCA (196) 591 chr1: chr1: GAAGAACAGGAT GAAGAACAGGAT 0 11 3.58 1.74E−02 3′ss Mel. 219366593-219383856 219366593-219383873 ATTAATAGTATG ATTAATAGGAGG TTTTTGTTTTTA ATTCTCTATGGG GGAG (894) AGGA (895) 592 chr19: chr19: CAAGCAGGTCCA CAAGCAGGTCCA 0 10 3.46 2.28E−04 3′ss Mel. 5595521-5598803 5595508-5598803 AAGAGAGATTTT AAGAGAGAAGCT GGTAAACAGAGC CCAAGAGTCAGG TCCA (138) ATCG (139) 593 chr5: chr5: CAATTCAGTAGA AGGTCTTCCTGG 0 10 3.46 2.42E−02 5′ss Mel. 462644-464404 462422-464404 TTCACCCTCAAC ACCTGGAGCAAC ATCTGAATGAAT ATCTGAATGAAT TGAT (896) TGAT (897) 594 chr9: chr9: GGGAGATGGATA GGGAGATGGATA 3 41 3.39 1.97E−10 3′ss Mel. 35813153-35813262 35813142-35813262 CCGACTTGCTCA CCGACTTGTGAT ATTTCAGTGATC CAACGATGGGAA AACG (146) GCTG (147) 595 chr1: chr1: AGAGGGCACGGG AGAGGGCACGGG 2 29 3.32 1.42E−03 3′ss Mel. 205240383-205240923 205240383-205240940 ACATCCAGCCCC ACATCCAGGAGG TCTGCCCCTGCA CCGTGGAGTCCT GGAG (898) GCCT (899) 596 chr11: chr11: TTCTCCAGGACC TTCTCCAGGACC 0 9 3.32 6.24E−03 3′ss Mel. 125442465-125445146 125442465-125445158 TTGCCAGACCTT TTGCCAGAGGAA TTCTATAGGGAA TCAAAGACTCCA TCAA (150) TCTG (151) 597 chr11: chr11: GGATGACCGGGA GGATGACCGGGA 0 9 3.32 3.79E−04 3′ss Mel. 71939542-71939690 71939542-71939770 TGCCTCAGTCAC TGCCTCAGATGG TTTACAGCTGCA GGAGGATGAGAA TCGT (47) GCCC (48) 598 chr16: chr16: AGATGATTGAGG AGATGATTGAGG 0 9 3.32 1.06E−02 3′ss Mel. 70292147-70292882 70292120-70292882 CAGCCAAGCTCT CAGCCAAGGCCG TTTCTGTCTTCT TCTATACCCAGG TGGT (900) ATTG (901) 599 chr2: chr2: GAGGAGCCACAC GAGGAGCCACAC 0 9 3.32 2.20E−02 3′ss Mel. 220044485-220044888 220044485-220044831 TCTGACAGATAC TCTGACAGTGAG CTGGCTGAGAGC GGTGCGGGGTCA TGGC (107) GGCG (108) 600 chr3: chr3: GCTGCTCTCTTC GCTGCTCTCTTC 0 9 3.32 2.87E−06 3′ss Mel. 45043100-45046767 45043100-45046782 AATACAAGTGCT AATACAAGGATA TCTGCTTCCAGG CCAAGGGTTCGA ATAC (902) GTTT (903) 601 chr9: chr9: AATAGAACTTCC AATAGAACTTCC 7 76 3.27 4.47E−08 3′ss Mel. 101891382-101894778 101891382-101894790 AACTACTGGCCC AACTACTGTAAA TTTTTCAGTAAA GTCATCACCTGG GTCA (904) CCTT (905) 602 chr17: chr17: CTATTTCACTCT CTATTTCACTCT 2 27 3.22 1.02E−05 3′ss Mel. 7131030-7131295 7131102-7131295 CCCCCGAACCTA CCCCCGAAATGA TCCAGGTTCCTC GCCCATCCAGCC CTCC (33) AATT (34) 603 chr17: chr17: TGTTACTGCAGT TGTTACTGCAGT 1 17 3.17 2.33E−03 3′ss Mel. 79556145-79563141 79556130-79563141 GGCTACAGGTCT GGCTACAGGTGG CTCTCTTGCAGG TCCTGACAACCA TGGT (906) AGTC (907) 604 chr13: chr13: ACATCACAAAGC ACATCACAAAGC 0 8 3.17 1.95E−03 3′ss Mel. 45841511-45857556 45841511-45857576 AACCTGTGGGGT AACCTGTGGTGT TTTGTTTTTGTT ACCTGAAGGAAA TTAG (908) TCTT (909) 605 chr14: chr14: GGTGCTGGCTGC GGTGCTGGCTGC 0 8 3.17 3.94E−03 3′ss Mel. 105176525-105177255 105176525-105177273 CTGCGAAACCCT CTGCGAAAGCCT GGCTGCCCCTGC GCTCACCAGCCG AGGC (910) CCAG (911) 606 chr16: chr16: CACCAAGCAGAG CACCAAGCAGAG 0 8 3.17 7.87E−04 3′ss Mel. 15129410-15129852 15129410-15129872 GCTTCCAGTCTG GCTTCCAGGCCA TCTGCCCTTTCT GAAGCCTTTTAA GTAG (216) AAGG (217) 607 chr17: chr17: CCTCTCTGCTCG CCTCTCTGCTCG 0 8 3.17 7.21E−08 3′ss Mel. 17062316-17064532 17062316-17064553 AGAAGGAGTGTG AGAAGGAGCTGG TGTCTTTTTGCC AGCAGAGCCAGA AACA (912) AGGA (913) 608 chr19: chr19: ATCACAACCGGA ATCACAACCGGA 0 8 3.17 1.45E−02 3′ss Mel. 15491444-15507960 15491423-15507960 ACCGCAGGCTCC ACCGCAGGCTCA TTCTGCCCTGCC TGATGGAGCAGT CGCA (661) CCAA (662) 609 chr3: chr3: CTGGAAGCTCAA CTGGAAGCTCAA 0 8 3.17 4.68E−04 3′ss Mel. 112724877-112727017 112724851-112727017 GGTACTAGATTT GGTACTAGTTTG TTCCTCTCTCTG CCAAAGAAACTA TCTT (914) GAGT (915) 610 chr1: chr1: CCCGAGCTCAGA CCCGAGCTCAGA 4 41 3.07 3.31E−04 3′ss Mel. 3548881-3549961 3548902-3549961 GAGTAAATTCTC GAGTAAATATGA CTTACAGACACT GATCGCCTCTGT GAAA (177) CCCA (178) 611 chr2: chr2: TATCCATTCCTG TATCCATTCCTG 1 15 3.00 3.44E−05 3′ss Mel. 178096758-178097119 178096736-178097119 AGTTACAGTATA AGTTACAGTGTC AACTTCCTTCTC TTAATATTGAAA ATGC (156) ATGA (157) 612 chr11: chr11: CGGCGATGACTC CGGCGATGACTC 0 7 3.00 2.48E−02 3′ss Mel. 62554999-62556481 62554999-62556494 GGACCCAGCTTC GGACCCAGGGCT TCTCCACAGGGC CCTTCAGTGGTA TCCT (916) GATG (917) 613 chr15: chr15: CCGCCAGGAGAA CCGCCAGGAGAA 0 7 3.00 9.38E−04 3′ss Mel. 41102168-41102274 41102168-41102268 CAAGCCCATCCC CAAGCCCAAGTT CTCACAGGCAGA AGTCCCCTCACA GATA (918) GGCA (919) 614 chr16: chr16: CAGCAGCAGCTC CAGCAGCAGCTC 0 7 3.00 9.09E−03 3′ss Mel. 48311390-48330007 48311390-48329925 TGCTTGAGCTAC TGCTTGAGGTGT TGCCAACACCAC TGGATCCTGAAC TGCT (920) AAAA (921) 615 chr2: chr2: AGACAAGGGATT AGACAAGGGATT 0 7 3.00 6.35E−04 3′ss Mel. 26437445-26437921 26437430-26437921 GGTGGAAACATT GGTGGAAAAATT TTATTTTACAGA GACAGCGTATGC ATTG (295) CATG (296) 616 chr3: chr3: GCACTTATGGTG GCACTTATGGTG 0 7 3.00 1.74E−07 3′ss Mel. 48638222-48638407 48638273-48638407 GTGGCGTGAGTT GTGGCGTGCACC TCCAGACCTTCA TGTCCAGCCCAC GCAT (922) TGGC (923) 617 chr19: chr19: GTGCTTGGAGCC GTGCTTGGAGCC 4 35 2.85 1.91E−07 3′ss Mel. 55776746-55777253 55776757-55777253 CTGTGCAGACTT CTGTGCAGCCTG TCCGCAGGGTGT GTGACAGACTTT GCGC (179) CCGC (180) 618 chr9: chr9: GTGGCTCCAGTA GACCTGCTCAAG 8 63 2.83 2.74E−02 5′ss Mel. 119414072-119488049 119414072-119449344 TCAGAAAGAGAC TTCACTCAAGAC CACAGAGCTGGG CACAGAGCTGGG CAGC (924) CAGC (925) 619 chr10: chr10: TGTGGGCATGGA TGTGGGCATGGA 0 6 2.81 8.27E−08 3′ss Mel. 82264534-82266954 82264534-82266983 GCGAAAAGTGCT GCGAAAAGGGTG GCCCTGCTTTCT TGCTGTCCGACC CTGT (926) TCAC (927) 620 chr12: chr12: TTCCTCTTCCCC TTCCTCTTCCCC 0 6 2.81 4.32E−06 3′ss Mel. 56361953-56362539 56361953-56362561 TCATCAAGTCCT TCATCAAGAGCT CTCTTTCTCCTT ATCTGTTCCAGC TGTC (928) TGCT (929) 621 chr19: chr19: GGGGCACTGACA GGGGCACTGACA 0 6 2.81 2.67E−02 3′ss Mel. 50149459-50149761 50149459-50149782 CGGCTACTAGCC CGGCTACTGTGT TCTCTGGCCTCT TGGACATGGCCA TCCA (930) CGGA (931) 622 chr20: chr20: ACATGAAGGTGG ACATGAAGGTGG 0 6 2.81 1.25E−04 3′ss Mel. 34144042-34144761 34144042-34144743 ACGGAGAGTTCT ACGGAGAGGTAC CTGTGACCAGAC TGAGGACAAATC ATGA (250) AGTT (50) 623 chrX: chrX: TGACTCCGCTGC TGACTCCGCTGC 0 6 2.81 1.80E−02 3′ss Mel. 118923962-118925536 118923974-118925536 TCGCCATGACTT TCGCCATGTCTT TCAGGATTAAGC CTCACAAGACTT GATT (697) TCAG (698) 624 chr2: chr2: CCCCTGAGATGA CCCCTGAGATGA 3 25 2.70 6.46E−06 exon Mel. 27260570-27260682 27260570-27261013 AGAAAGAGCTCC AGAAAGAGCTCC incl. CTGTTGACAGCT TGAGCAGCCTGA GCCT (183) CTGA (184) 625 chr2: chr2: AGGCTGTAGCAG AGGCTGTAGCAG 1 12 2.70 2.24E−02 3′ss Mel. 99225189-99226105 99225189-99226218 GACTCCAGGGTT GACTCCAGGAAG GGGAAGAACATG ATGTTACCGAGT GAAA (932) ACTT (933) 626 chr8: chr8: CCGAGGATGCTA CCGAGGATGCTA 4 30 2.63 6.42E−03 3′ss Mel. 133811106-133811328 133811106-133816063 AGGGGCAGTTTC AGGGGCAGGATT TGTTCCAGGTGA GGATAGCTTTAG AATC (934) TCAA (935) 627 chr21: chr21: GCCTCCCGGTCC GCCTCCCGGTCC 4 29 2.58 9.60E−04 3′ss Mel. 46935066-46945730 46936054-46945730 GCAAGCAGAATG GCAAGCAGTTCC AAGAACTGCATG AGTTATACTCCG TGGC (936) TGTA (937) 628 chr17: chr17: TCGTAACAGGGG CTGTGACGGGTG 3 23 2.58 1.22E−02 exon Mel. 27210249-27212874 27210249-27211242 TTGCACAGGTGA TCGCCCAGGTGA skip AGATCATGACGG AGATCATGACGG AGAA (938) AGAA (939) 629 chr6: chr6: GTTTGGGGAAGT GTTTGGGGAAGT 1 11 2.58 2.07E−05 exon Mel. 112020873-112021306 112017659-112021306 ATGGATGGAGAA ATGGATGGGTAC incl. AGCTGATGGTTT CTGGAATGGAAA GTGT (940) CACA (941) 630 chr6: chr6: TAACTAATCCTT CAGCCTACCAGA 1 11 2.58 4.06E−02 5′ss Mel. 39854223-39855261 39851845-39855261 CTCAGCAGAAAG GGCACCAGAAAG AGCTGGGCTCCA AGCTGGGCTCCA CTGA (942) CTGA (943) 631 chr11: chr11: AGTCCAGCCCCA AGTCCAGCCCCA 0 5 2.58 9.35E−03 3′ss Mel. 64900740-64900940 64900723-64900940 GCATGGCACCTC GCATGGCAGTCC TCCCCACTCCTA TGTACATCCAGG GGTC (136) CCTT (137) 632 chr16: chr16: GGATCCTTCACC GGATCCTTCACC 0 5 2.58 1.87E−03 3′ss Mel. 1402307-1411686 1402307-1411743 CGTGTCTGTCTT CGTGTCTGGACC TGCAGACAGGTT CGTGCATCTCTT CTGT (85) CCGA (86) 633 chr17: chr17: GCATCTCAGCCC GCATCTCAGCCC 0 5 2.58 1.16E−05 3′ss Mel. 16344444-16344670 16344444-16344681 AAGAGAAGTTTC AAGAGAAGGTTA TTTGCAGGTTAT TATTCCCAGAGG ATTC (287) ATGT (288) 634 chr1: chr1: CTACACAGAGCT CTACACAGAGCT 0 5 2.58 2.48E−06 3′ss Mel. 32096333-32098095 32096443-32098095 GCAGCAAGGTGT GCAGCAAGCTCT GCACCCAGCTGC GTCCCAAATGGG AGGT (291) CTAC (292) 635 chr22: chr22: CCTGCGCAACTG CCTGCGCAACTG 0 5 2.58 1.56E−04 3′ss Mel. 19164146-19164358 19164206-19164358 GTACCGAGGCGC GTACCGAGGGGA AGCCAGTGTCTT CAACCCCAACAA TGGA (944) GCCC (945) 636 chr3: chr3: ATAAAAATTGCT ATAAAAATTGCT 0 5 2.58 2.28E−03 3′ss Mel. 131181737-131186934 131181719-131186934 TAGTAAAGATTT TAGTAAAGGTCA TTGCCTTCTCTC AAGATTCTAAAC AGGT (946) TGCC (947) 637 chr8: chr8: TGAGTTCATGGA TGAGTTCATGGA 0 5 2.58 3.48E−02 3′ss Mel. 98817692-98827531 98817692-98827555 TGATGCCAAAAT TGATGCCAACAT TCTTTTTAATCT GTGCATTGCCAT TTCG (948) TGCG (949) 638 chrX: chrX: AGAGTTGAAAAA AGAGTTGAAAAA 0 5 2.58 4.97E−03 3′ss Mel. 24091380-24092454 24091380-24094838 CACTGGCGTCTC CACTGGCGTTTA CTTTTCAGGAAT ATTGGTTGGGGT CACA (950) CAGA (951) 639 chr12: chr12: GGCCAGCCCCCT GGCCAGCCCCCT 8 51 2.53 3.07E−09 3′ss Mel. 120934019-120934204 120934019-120934218 TCTCCACGGCCT TCTCCACGGTAA TGCCCACTAGGT CCATGTGCGACC AACC (206) GAAA (207) 640 chr9: chr9: CACCACGCCGAG CACCACGCCGAG 3 21 2.46 2.87E−02 3′ss Mel. 125023777-125026993 125023787-125026993 GCCACGAGACAT GCCACGAGTATT TGATGGAAGCAG TCATAGACATTG AAAC (142) ATGG (143) 641 chr10: chr10: TGGGGCCACAAA TGGGGCCACAAA 4 24 2.32 1.77E−02 exon Mel. 74994698-74999069 74994698-74994950 GACAGATGCTGG GACAGATGAAAC skip ATACACAGTATC CCCATGGCGACT GTCG (952) CTAG (953) 642 chr1: chr1: CTTGCCTTCCCA CTTGCCTTCCCA 1 9 2.32 1.49E−04 3′ss Mel. 154246074-154246225 154246074-154246249 TCCTCCTGCAAA TCCTCCTGAACT CACCTGCCACCT TCCAGGTCCTGA TTCT (289) GTCA (290) 643 chr11: chr11: GGGGACAGTGAA GGGGACAGTGAA 0 4 2.32 1.19E−05 3′ss Mel. 57100545-57100908 57100623-57100908 ATTTGGTGGCAA ATTTGGTGGGCA GAATGAGGTGAC GCTGCTTTCCTT ACTG (103) TGAC (104) 644 chr16: chr16: GAACTGGCACCG GAACTGGCACCG 0 4 2.32 1.03E−03 3′ss Mel. 313774-313996 313774-314014 ACAGACAGTGTC ACAGACAGATCC CCCTCCCTCCCC TGTTTCTGGACC AGAT (244) TTGG (245) 645 chr17: chr17: AACATGGAATCA AACATGGAATCA 0 4 2.32 1.03E−03 3′ss Mel. 34147441-34149625 34147441-34149643 TCAGGAAGTTCT TCAGGAAGCCAA CCATTTCTATTT GGTGGAAGAGCA AGCC (954) CCTT (955) 646 chr1: chr1: CGTGCGTGTGTG CTTAGGAAAGAC 0 4 2.32 2.87E−02 5′ss Mel. 1480382-1497319 1480382-1500152 TGCTCTTGCTAT AAAGAACTCTAT ACACAGAATGGG ACACAGAATGGG ATTT (956) ATTT (957) 647 chr22: chr22: CCCAGCCTGCTG CCCAGCCTGCTG 0 4 2.32 3.33E−02 3′ss Mel. 24108483-24109560 24108462-24109560 TCCAGCAGCCTC TCCAGCAGGCCC TTGCACTGTACC CCACCCCCGCTG CCCA (958) CCCC (959) 648 chr22: chr22: ACCCAAGGCTCG ACCCAAGGCTCG 0 4 2.32 5.75E−03 3′ss Mel. 44559810-44564460 44559810-44564481 TCCTGAAGTTTC TCCTGAAGACGT TCTGTTTCCTTC GGTTAACTTGGA TGCA (960) CCTC (961) 649 chr5: chr5: AGATTGAAGCTA AGATTGAAGCTA 0 4 2.32 1.38E−03 3′ss Mel. 132439718-132439902 132439718-132439924 AAATTAAGTTTT AAATTAAGGAGC CTGTCTTACCCA TGACAAGTACTT TTCC (348) GTAG (349) 650 chr5: chr5: GAACCCGGTGGT GAACCCGGTGGT 0 4 2.32 5.33E−04 3′ss Mel. 175815974-175816311 175815974-175816331 ACCCATAGTTGC ACCCATAGGTTG TTTGTCCCCTCC CCTGGCCACGGC TCAG (962) GGCC (963) 651 chr7: chr7: AATGGAAGTACC AATGGAAGTACC 0 4 2.32 7.50E−03 3′ss Mel. 74131270-74133179 74131270-74133197 AGCAGAAGAATT AGCAGAAGATTC TTATTTTTTTCA TACTCAACATGT AGAT (964) CCCT (965) 652 chr20: chr20: GGCAGCTGTTAG GGCAGCTGTTAG 7 37 2.25 4.91E−02 exon Mel. 57227143-57234678 57227143-57242545 CCGAGCAAGAGC CCGAGCAACTTG incl. TGGACGAGGTAT CTGATGACCGTA TGTG (966) TGGC (967) 653 chr16: chr16: GAGATTCTGAAG GAGATTCTGAAG 3 18 2.25 1.03E−03 3′ss Mel. 54954250-54957496 54954322-54957496 ATAAGGAGTTCT ATAAGGAGGTAA CTTGTAGGATGC AACCTGTTTAGA CACT (313) AATT (314) 654 chrX: chrX: AAAAGAAACTGA AAAAGAAACTGA 14 70 2.24 5.98E−06 3′ss Mel. 129771378-129790554 129771384-129790554 GGAATCAGTATC GGAATCAGCCTT ACAGGCAGAAGC AGTATCACAGGC TCTG (303) AGAA (304) 655 chr13: chr13: GTTTAGAAATGG GTTTAGAAATGG 18 88 2.23 1.12E−04 3′ss Mel. 45911538-45912794 45911523-45912794 AAAAATGTTTTT AAAAATGTTAAC TGCTTTTACAGT AAATGTGGCAAT AACA (968) TATT (969) 656 chr2: chr2: CCAAGAGACAGC CCCCTGAGATGA 5 27 2.22 4.64E−05 exon Mel. 27260760-27261013 27260570-27261013 ACATTCAGCTCC AGAAAGAGCTCC incl. TGAGCAGCCTGA TGAGCAGCCTGA CTGA (315) CTGA (184) 657 chr1: chr1: TTGGAAGCGAAT TTGGAAGCGAAT 1 8 2.17 6.85E−03 3′ss Mel. 23398690-23399766 23398690-23399784 CCCCCAAGTCCT CCCCCAAGTGAT TTGTTCTTTTGC GTATATCTCTCA AGTG (210) TCAA (211) 658 chr6: chr6: AGGATGTGGCTG AGGATGTGGCTG 1 8 2.17 2.70E−05 3′ss Mel. 31602334-31602574 31602334-31602529 GCACAGAAGTGT GCACAGAAATGA CATCAGGTCCCT GTCAGTCTGACA GCAG (148) GTGG (149) 659 chr3: chr3: AAATCTCGTGGA AAATCTCGTGGA 7 33 2.09 4.05E−02 3′ss Mel. 16310782-16312435 16310782-16312451 CTTCTAAGTTTT CTTCTAAGAAAG CTGTTTGCCCAG CGCCATGGCCTG AAAG (970) TGCT (971) 660 chr11: chr11: AGTTCCGGGGCT AGTTCCGGGGCT 0 3 2.00 2.75E−02 3′ss Mel. 68838888-68839375 68838888-68839390 ACCTGATGCCTT ACCTGATGAAAT CCTCTTTGCAGA CTCTCCAGACCT AATC (972) CGCT (973) 661 chr12: chr12: GGCACCCCAAAA GGCACCCCAAAA 0 3 2.00 1.12E−02 3′ss Mel. 58109976-58110164 58109976-58110194 GATGGCAGATCA GATGGCAGGTGC GTCTCTCCCTGT GAGCCCGACCAA TCTC (285) GGAT (286) 662 chr1: chr1: AAGAAGGAATCC AAGAAGGAATCC 0 3 2.00 7.34E−03 3′ss Mel. 32377442-32381495 32377427-32381495 ACGTTCTAGTCA ACGTTCTAGATT TTTCTTTTCAGG GGCCATTTGATG ATTG (974) ATGG (975) 663 chr22: chr22: CGCTGGCACCAT CGCTGGCACCAT 0 3 2.00 2.55E−02 3′ss Mel. 36627471-36629198 36627512-36629198 GAACCCAGGACC GAACCCAGAGAG AAGTGAGCAGAG CAGTATCTTTAT AGAA (976) TGAG (200) 664 chr3: chr3: GCAACCAGTTTG GCAACCAGTTTG 0 3 2.00 3.20E−03 3′ss Mel. 49395199-49395459 49395180-49395459 GGCATCAGCTGC GGCATCAGGAGA CCTTCTCTCCTG ACGCCAAGAACG TAGG (342) AAGA (343) 665 chr6: chr6: AGCCCCTGCTTG AGCCCCTGCTTG 0 3 2.00 4.68E−04 3′ss Mel. 170844509-170846321 170844493-170846321 ACAACCAGTTTC ACAACCAGGTTG ATGTCCCACCAG GTTTTAAGAACA GTTG (977) TGCA (978) 666 chr9: chr9: CCAAGGACTGCA CCAAGGACTGCA 0 3 2.00 4.46E−02 3′ss Mel. 139837449-139837800 139837395-139837800 CTGTGAAGGCCC CTGTGAAGATCT CCGCCCCGCGAC GGAGCAACGACC CTGG (175) TGAC (176) 667 chr10: chr10: TTGGCTGTAGGA TTGGCTGTAGGA 8 34 1.96 2.70E−05 exon Mel. 103904064-103908128 103904064-103904776 AACTCAGGGTCC AACTCAGGCGGC skip AGCTGTAGTTCC GTTGACATTCCC TCTG (979) CAGG (980) 668 chr17: chr17: TGTATCTCCGAC TGTATCTCCGAC 6 26 1.95 3.79E−02 exon Mel. 27212965-27215962 27211333-27215962 ACTCAGAGACTG ACTCAGAGGATT incl. TCTCTGGAGGTT TCCCTAGAGATT ATGA (981) ATGA (982) 669 chrX: chrX: AGGCTGATCTAC AGGCTGATCTAC 2 10 1.87 5.30E−03 3′ss Mel. 15849691-15863501 15845495-15863501 TGCAGGAGCCAC TGCAGGAGGAAG GTCATGAATATT CTGAAACCCCAC TTAA (983) GTAG (984) 670 chr2: chr2: GGAAATGGGACA GGAAATGGGACA 14 52 1.82 4.43E−06 3′ss Mel. 230657846-230659894 230657861-230659894 GGAGGCAGAGGA GGAGGCAGCTTT TCACAGGCTTTA TCTCTCAACAGA AAAT (387) GGAT (388) 671 chr5: chr5: GCTCAGCCCCCT TGACCCTGCAGC 5 20 1.81 2.74E−03 exon Mel. 141694720-141699308 141694720-141704408 CCCCACAGGGCC TCCTCAAAGGCC incl. CCTAGAAGCCTG CCTAGAAGCCTG TTTC (985) TTTC (986) 672 chr19: chr19: GCCGACCCGCCT GCCGACCCGCCT 3 13 1.81 4.16E−03 3′ss Mel. 3542975-3544806 3544730-3544806 GCGACGCTCTTT GCGACGCTGGGA TCTTGCCTGGAG CCGTGATGCCCG AAGA (987) GCCC (988) 673 chr3: chr3: TGCGGAGACCCC TGCGGAGACCCC 1 6 1.81 2.67E−02 exon Mel. 58417711-58419494 58419411-58419494 TTCGGGAGGTGA TTCGGGAGGTCT skip CAGTTCGTGATG CCGGGCTGCTGA CTAT (989) AGAG (990) 674 chr6: chr6: CTATCAGTAGGT GCATTGATGTGG 1 6 1.81 2.71E−03 exon Mel. 108370622-108370735 108370622-108372234 TTTTAGAGATGA AAGATGCAATGA incl. ACATCACTCGAA ACATCACTCGAA AACT (991) AACT (992) 675 chr6: chr6: GCATTGATGTGG GCATTGATGTGG 1 6 1.81 1.84E−03 exon Mel. 108370787-108372234 108370622-108372234 AAGATGCAGTTT AAGATGCAATGA incl. TTTTCCTGGCAG ACATCACTCGAA AAGA (993) AACT (992) 676 chr6: chr6: CAGTGGGCGGAT CAGTGGGCGGAT 1 6 1.81 1.04E−02 3′ss Mel. 166779550-166780282 166779594-166780282 GACATTTGGTAC GACATTTGCCCT AGCCTCGGAACT CTGTTGCTATTC GGCT (994) TTTG (995) 677 chr7: chr7: GGTGTCCATGGC GGTGTCCATGGC 1 6 1.81 4.73E−02 exon Mel. 128033792-128034331 128033082-128034331 CTGCACTCCTAT CTGCACTCTTAC incl. ACCTTTCTGCCG GAAAAGCGGCTG TGTA (996) TACT (997) 678 chr6: chr6: ACTGGGAAGTTC ACTGGGAAGTTC 10 37 1.79 1.30E−02 exon Mel. 136597127-136599002 136597646-136599002 TTAAAAAGTCCC TTAAAAAGGTTC skip CCTCTACACAAG ACAGATGAAGAG AATC (998) TCTA (999) 679 chr16: chr16: GAGATTCTGAAG GAGATTCTGAAG 20 69 1.74 1.28E−05 3′ss Mel. 54954239-54957496 54954322-54957496 ATAAGGAGGATG ATAAGGAGGTAA CCACTGGAAATG AACCTGTTTAGA TTGA (322) AATT (314) 680 chr4: chr4: GCTGAGCGGGGC TCCAACAAGCAC 20 69 1.74 4.13E−05 exon Mel. 17806394-17812069 17806394-17806729 GACCCGAGTCTT CTCTGAAGTCTT skip CTCATTCACAGG CTCATTCACAGG TTAA (1000) TTAA (832) 681 chr19: chr19: AGTGGCAGTGGC AGTGGCAGTGGC 8 29 1.74 8.03E−04 3′ss Mel. 6731065-6731209 6731122-6731209 TGTACCAGCCCA TGTACCAGCTCT CAGGAAACAACC TGGTGGAGGGCT CGTA (311) CCAC (312) 682 chr16: chr16: TGTTCCACCTCC TGTTCCACCTCC 6 22 1.72 2.96E−02 3′ss Mel. 28842393-28843507 28842393-28843525 TCCTGCAGCTCC TCCTGCAGTGGG CCCTTTTCTTCC CCGGATGTATCC AGTG (1001) CCCG (1002) 683 chr3: chr3: ACCCATGAGAAT CTGGCCCCTGAG 8 28 1.69 8.95E−03 exon Mel. 50615004-50617274 50616357-50617274 GCTCAGAGCTAT ATCCGCAGCTAT skip GAAGACCCCGCG GAAGACCCCGCG GCCC (1003) GCCC (1004) 684 chr11: chr11: CAAGCTCGAGTC CAAGCTCGAGTC 4 15 1.68 8.31E−03 exon Mel. 772521-774007 773629-774007 CATCGATGAACC CATCGATGGTGC skip CATCTGCGCCGT CCGGTACCATGC CGGC (1005) CCTC (1006) 685 chr2: chr2: CTTCACTGTCAC CTTCACTGTCAC 9 30 1.63 2.25E−02 3′ss Mel. 220424219-220427123 220426730-220427123 CGTCACAGAACC CGTCACAGAGTC CCCAGTGCGGAT TTACCAAAGTCA CATA (1007) GGAC (1008) 686 chr3: chr3: GTCTTCCAATGG GTCTTCCAATGG 10 33 1.63 1.04E−02 3′ss Mel. 148759467-148759952 148759455-148759952 CCCCTCAGCCTT CCCCTCAGGAAA TTCTCTAGGAAA TGATACACCTGA TGAT (234) AGAA (235) 687 chr5: chr5: AGAAACAGAAAC AGAAACAGAAAC 5 17 1.58 1.55E−02 exon Mel. 34945908-34949647 34945908-34950274 CAGCACAGGATG CAGCACAGAATT incl. TACCTGGCAAAG ATGATGACAATT ATTC (1009) TCAA (1010) 688 chr6: chr6: TTCTGCATCTGT AAAGGAGTGCTT 2 8 1.58 1.45E−02 exon Mel. 158589427-158613008 158591570-158613008 GGGCCGAGTGAT ATAGAATGTGAT skip CCTGCCATGAAG CCTGCCATGAAG CAGT (1011) CAGT (1012) 689 chr14: chr14: AGGATCGGCAAC CTGGGATAAGAG 1 5 1.58 1.98E−02 exon Mel. 23495584-23496953 23495584-23502576 ATGGCAAGGCCT AGGCCCTGGCCT incl. CTACTACGTGGA CTACTACGTGGA CAGT (1013) CAGT (1014) 690 chr6: chr6: GTTCAGGACACA GGGAGGGAGAGA 1 5 1.58 1.23E−02 exon Mel. 33669197-33678471 33669197-33679325 ATAAGCAGGTTG ATACCCAGGTTG incl. CAGAGCCTGAGG CAGAGCCTGAGG CCTG (1015) CCTG (1016) 691 chr10: chr10: TACCCGGATGAT TACCCGGATGAT 0 2 1.58 2.58E−04 3′ss Mel. 102286851-102289136 102286831-102289136 GGCATGGGAAGT GGCATGGGGTAT TCTTGCTGTCTT GGCGACTACCCG TCAG (1017) AAGC (1018) 692 chr11: chr11: GACATATGAGTC GACATATGAGTC 0 2 1.58 2.45E−02 3′ss Mel. 66333872-66334716 66333875-66334716 AAAGGAAGCCCG AAAGGAAGAAGC GTGGCGCCTGTC CCGGTGGCGCCT CGTC (1019) GTCC (1020) 693 chr11: chr11: CGGATCAACTTC CGGATCAACTTC 0 2 1.58 2.65E−03 3′ss Mel. 8705628-8706243 8705628-8706264 GACAAATAGTGG GACAAATACCAC TTGTTACCTCTT CCAGGCTACTTT CCTA (1021) GGGA (1022) 694 chr12: chr12: TTATAGGCGTGA TTATAGGCGTGA 0 2 1.58 1.03E−03 3′ss Mel. 53421972-53427574 53421972-53427589 TGATAGAGTTTC TGATAGAGGTCC ATTTAACTTAGG CCCCCAAAGACC TCCC (1023) CAAA (1024) 695 chr15: chr15: TGGAAATATTTC GCCTCACTGAGC 0 2 1.58 7.87E−03 exon Mel. 25212387-25213078 25207356-25213078 TAGACTTGGTGT AACCAAGAGTGT incl. CAGTTGTACCCG CAGTTGTACCCG AGGC (1025) AGGC (145) 696 chr1: chr1: TCGGCCCAGAAG CTTAGGAAAGAC 0 2 1.58 4.66E−02 5′ss Mel. 1480382-1497338 1480382-1500152 AACCCCGCCTAT AAAGAACTCTAT ACACAGAATGGG ACACAGAATGGG ATTT (1026) ATTT (957) 697 chr5: chr5: TCTATATCCCCT TCTATATCCCCT 0 2 1.58 1.26E−04 3′ss Mel. 177576859-177577888 177576839-177577888 CTAAGACGCACT CTAAGACGGACC TCTTTCCCCTCT TGGGTGCAGCCG GTAG (299) CAGG (300) 698 chr6: chr6: GCTGAAGGGAAA GCTGAAGGGAAA 0 2 1.58 4.68E−02 3′ss Mel. 42905945-42911535 42905945-42906305 AGACACCAAAAC AGACACCAGTTG ACAAACAGCAGA CCTGGCAGAGCA ATGG (1027) GTGG (1028) 699 chr17: chr17: CATCATCAAGTT CATCATCAAGTT 5 16 1.50 1.74E−04 intron Mel. 2282497-2282499 2282497-2282725 TTTCAATGACGA TTTCAATGAACG reten- GCTGGTCCAGCC TGCTGAGCATCA tion ATCC (1029) CGAT (1030) 700 chr8: chr8: GAGGGCCTGCTC ACATGCTTCAAA 23 66 1.48 1.49E−03 exon Mel. 74601048-74621266 74601048-74650518 ATTCAAAGATGT TAAATCAGATGT incl. TCTCAGTGCAGC TCTCAGTGCAGC TGAG (1031) TGAG (1032) 701 chr10: chr10: CTGAGGCTAATG CTGAGGCTAATG 14 40 1.45 2.13E−02 3′ss Mel. 35495979-35500583 35495979-35500181 AAAAACAGGGAA AAAAACAGGGAA GCTGCCAAAGAA GCTGCCCGGGAG TGTC (1033) TGTC (1034) 702 chr3: chr3: CGGCTGGGACTC CGGCTGGGACTC 12 34 1.43 1.81E−02 3′ss Mel. 119180951-119182182 119180995-119182182 TTCCATGCGTGG TTCCATGCAGTT CACTGGAAGCAG GAAACTGGTTGA ACTG (1035) CAAC (1036) 703 chr4: chr4: AGTGAATGTAGT AGTGAATGTAGT 17 47 1.42 2.45E−02 exon Mel. 169919436-169923221 169911479-169923221 TGCACCAGTGAC TGCACCAGGATT incl. AATACTTGTATG TGTACACACAGA GAGT (1037) TATG (1038) 704 chr17: chr17: ATTCACACAGAG TGAGGATCAATC 2 7 1.42 1.30E−02 exon Mel. 55074416-55078215 55075859-55078215 CCACCTAGGCCA CTGGGGAGGCCA skip GGCTACCAACGT GGCTACCAACGT CTTT (1039) CTTT (1040) 705 chrX: chrX: AGAAACCTTGAA AGAAACCTTGAA 7 20 1.39 3.40E−02 exon Mel. 2310515-2326785 2209644-2326785 CGACAAAGAGAC CGACAAAGTGGA incl. GTGAGTCTTGCT ATTTTTATACTG GTGT (496) TGAC (495) 706 chrY: chrY: AGAAACCTTGAA AGAAACCTTGAA 7 20 1.39 3.40E−02 exon Mel. 2260515-2276785 2159644-2276785 CGACAAAGAGAC CGACAAAGTGGA incl. GTGAGTCTTGCT ATTTTTATACTG GTGT (496) TGAC (495) 707 chr5: chr5: TGGAAAAGTATA TGGAAAAGTATA 4 12 1.38 2.71E−02 exon Mel. 54456224-54459882 54456224-54456821 AAGGCAAAATTC AAGGCAAAGTTT skip TTCAAAGAAGGA CACTAGTTGTAA ACCA (1041) ACGT (1042) 708 chr15: chr15: ATACTAAGAACA ATACTAAGAACA 19 50 1.35 2.54E−02 exon Mel. 76146828-76161291 76146828-76152218 ACAATTTGAATG ACAATTTGCTTC skip GGACAACAGAAG GTCAGCAATTGA AAGT (1043) AGTG (1044) 709 chr8: chr8: TGGCCTTGACCT TGGCCTTGACCT 7 19 1.32 3.77E−02 3′ss Mel. 38270113-38271435 38271322-38271435 CCAACCAGGTCC CCAACCAGGAGT TGCACCCAGACC ACCTGGACCTGT TCAC (1045) CCAT (1046) 710 chr1: chr1: GAAGGCAGCTGA GAAGGCAGCTGA 3 9 1.32 1.42E−02 3′ss Mel. 11131045-11132143 11131030-11132143 GCAAACAGTTCT GCAAACAGCTGC CTCCCTTGCAGC CCGGGAACAGGC TGCC (393) AAAG (394) 711 chr11: chr11: TCCTTGAACACT TCCTTGAACACT 1 4 1.32 2.52E−02 exon Mel. 62556898-62557357 62556898-62557072 ACAATTAGACCT ACAATTAGCTGT skip CTTCTTGGGTGA TCTGAAGCCCAG ATTT (1047) AAAA (1048) 712 chr14: chr14: ACACCATTGAGG ACACCATTGAGG 1 4 1.32 1.92E−02 exon Mel. 69349309-69350884 69349772-69350884 AGATCCAGGTGC AGATCCAGGGAC skip GGCAGCTGGTGC TGACCACAGCCC CTCG (1049) ATGA (1050) 713 chr1: chr1: CCCATGTATAAG CCCATGTATAAG 1 4 1.32 2.77E−02 3′ss Mel. 155227125-155227288 155227177-155227288 GCTTTCCGGATG GCTTTCCGGAGT TGCTCTTTGTCC GACAGTTCATTC TCCA (1051) AATT (1052) 714 chr20: chr20: CTCCCAGTGCTG GAGCTGCCACGG 1 4 1.32 2.02E−02 exon Mel. 25281520-25281967 25281520-25282854 TATATCCCGGAA ATACTGAGGGAA incl. .TTCCTGGGGAAG TTCCTGGGGAAG TCGG (1053) TCGG (1054) 715 chr7: chr7: GGATGCGCGTCT AGCCGCAGAGCA 1 4 1.32 4.91E−02 exon Mel. 142962185-142964709 142962389-142964709 GGTCAAGGGCTG TCCTGGCGGCTG skip CAGAGAAGGCTG CAGAGAAGGCTG GTAT (1055) GTAT (1056) 716 chr8: chr8: ACATGCTTCAAA ACATGCTTCAAA 24 61 1.31 1.74E−02 exon Mel. 74621397-74650518 74601048-74650518 TAAATCAGCTTC TAAATCAGATGT incl. TCTCCAAGATAA TCTCAGTGCAGC AATG (1057) TGAG (1032) 717 chr15: chr15: AACAAAGAAATA CTGAGTCTTTAT 16 41 1.30 1.66E−03 exon Mel. 49309825-49319561 49309825-49311614 ATTCACAGGATG ATTTTGAGGATG skip AAGATGGGTTTC AAGATGGGTTTC AAGA (1058) AAGA (1059) 718 chrX: chrX: TAGCCACCACTG GGGAAAAGTCTT 11 28 1.27 1.07E−02 exon Mel. 148582568-148583604 148582568-148584841 TGTGCCAGGGAT TCACCCTGGGAT incl. ATCTTCTAACCA ATCTTCTAACCA TACC (1060) TACC (1061) 719 chr12: chr12: CCTACCAGCCAC CCTACCAGCCAC 4 11 1.26 2.42E−02 3′ss Mel. 49918679-49919860 49918679-49919726 TTCGGGAGGTAT TTCGGGAGGTAT CAGAGTGCTCCA TGCCAGGGAACA TCTC (1062) GACG (1063) 720 chr1: chr1: GTCCCGGCTTCC GTCCCGGCTTCC 4 11 1.26 2.67E−02 exon Mel. 46654652-46655129 46655029-46655129 CCCTACTCGCCT CCCTACTCAGTG skip GGCTCAGAATCT AAGAAGCCACCC AACC (1064) TCAG (1065) 721 chr3: chr3: CTTAAGCATATA CTTAAGCATATA 28 68 1.25 2.24E−02 exon Mel. 105397415-105400567 105400454-105400567 TTTAAAGGGTGA TTTAAAGGGAGA skip AGATGCTTTTGA TGTTTTTGATTC TGCC (1066) AGCC (1067) 722 chr3: chr3: CAGGAACAAGTA CAGGAACAAGTA 2 6 1.22 4.97E−02 exon Mel. 10023431-10028190 10019130-10028190 TCTGACAGAAAA TCTGACAGTCAA incl. TATCTTTCAGGC GTCCTAATTCGA CTGG (1068) AGCA (1069) 723 chr4: chr4: GAAGTTCTGAGG GAAGTTCTGAGG 2 6 1.22 1.07E−02 3′ss Mel. 88898249-88901544 88898249-88901197 AAAAGCAGAATG AAAAGCAGCTTT CTGTGTCCTCTG ACAACAAATACC AAGA (1070) CAGA (1071) 724 chr7: chr7: ATCTCCCTCTTG ATCTCCCTCTTG 2 6 1.22 1.94E−03 3′ss Mel. 23313233-23313672 23313233-23313683 GTGTACAAATTG GTGTACAAAAAA TTTTCAGAAAAC CACAAGGAATAC ACAA (1072) AACC (1073) 725 chr1: chr1: TGCGAGTACTGC TGCGAGTACTGC 6 15 1.19 3.00E−03 exon Mel. 214454770-214488104 214454770-214478529 TTCACCAGAAAG TTCACCAGGAAA skip AAGATTGGCCCA GAAGGATTGTCC TGCA (1074) AAAT (1075) 726 chr15: chr15: TCCAGAAAGTGA TCCAGAAAGTGA 15 35 1.17 2.02E−04 exon Mel. 101826006-101827112 101826498-101827112 AACTAAAATTTT AACTAAAAGAGC skip AATCCAGGTGCT GTCAGGAAGCAG GGTT (1076) AGAA (1077) 727 chr15: chr15: ACTCAGATGCCG ACTCAGATGCCG 39 88 1.15 2.54E−04 3′ss Mel. 74326871-74327483 74326871-74327512 AAAACTCGCCCT AAAACTCGTGCA CAGTCTGAGGTT TGGAGCCCATGG CTGT (748) AGAC (749) 728 chrX: chrX: AGATTCTACAGA AGATTCTACAGA 17 39 1.15 2.23E−02 exon Mel. 15706981-15720904 15706981-15711085 TAAATCAGATTT TAAATCAGCTGC skip CGGAAACTTCTG ACTTAGTGCATT GCAG (1078) GGAA (1079) 729 chr3: chr3: TGGCTGGCTTCA TGGCTGGCTTCA 40 90 1.15 1.67E−02 exon Mel. 183703166-183705557 183700795-183705557 GTGGACCAAATT GTGGACCAGCCT incl. TTCAGGATGGCT TCATGGTGAAAC GTAT (1080) ACCT (1081) 730 chr16: chr16: CCCTGCTCATCA CCCTGCTCATCA 19 40 1.04 9.38E−04 exon Mel. 684797-685280 684956-685280 CCTACGGGGAAC CCTACGGGCCCT skip CCAGAATGGGGG ATGCCATCAATG CTTC (1082) GGAA (194) 731 chrX: chrX: CAAACACCTCTT CAAACACCTCTT 11 23 1.00 2.44E−04 exon Mel. 123224614-123224703 123224614-123227867 GATTATAACACG GATTATAATCGG incl. CAGGTAACATGG CGTGGCACAAGC ATGT (468) CTAA (457) 732 chr20: chr20: GGCAGCCACCAC TGATAATTGGGC 10 21 1.00 2.87E−02 exon Mel. 48700791-48729643 48700791-48713208 GGGCTCGGACAA CTCCAAGAACAA skip TTTATGAAAACC TTTATGAAAACC GAAT (1083) GAAT (1084) 733 chr19: chr19: ACCGCCCTGCAC ACCGCCCTGCAC 7 15 1.00 2.95E−02 3′ss Mel. 617870-618487 617849-618487 TGCTACAGGAGT TGCTACAGGAAG CCTCCGCTCTGC GGCCTGACCTTC CACA (1085) GTCT (1086) 734 chr1: chr1: TCACAATTATAG GTGCTATTAAAG 7 15 1.00 1.48E−02 exon Mel. 220242774-220247308 220242774-220246191 GGGAAGAGCTCG AAGAAGATCTCG skip TGGTCTGGGTTG TGGTCTGGGTTG ATCC (1087) ATCC (1088) 735 chr1: chr1: CTCGTCTATGAT CTCGTCTATGAT 6 13 1.00 3.26E−02 3′ss Mel. 229431657-229433266 229431657-229433228 ATCACCAGATGC ATCACCAGCCGA CCGAATGCTAGC GAAACCTACAAT GAGC (1089) GCGC (1090) 736 chr11: chr11: CAATGCCACAGG CAATGCCACAGG 4 9 1.00 1.30E−02 3′ss Mel. 57193182-57193461 57193143-57193461 GCAGGCTGGAAG GCAGGCTGACTG GCTGGGATGCAT CAAAGCCCAGGA GGGA (1091) TGAG (1092) 737 chr11: chr11: TCAGAAGAGAAA TCAGAAGAGAAA 3 7 1.00 3.02E−02 3′ss Mel. 66105278-66105713 66105360-66105713 ATCGGATGACAG ATCGGATGGACC GCGGACCCACAG TTGACCCTGCTG GCCC (1093) TTCA (1094) 738 chr7: chr7: TGACTGCCGCTT CTAAAGCCTTCT 3 7 1.00 2.44E−02 exon Mel. 44251203-44251845 44250723-44251845 TCTCTCAGGCCC ATAAAACTGCCC incl. GGAAACAAAACT GGAAACAAAACT CATG (1095) CATG (1096) 739 chr12: chr12: ATGCAGATACAC ATGCAGATACAC 2 5 1.00 1.43E−02 exon Mel. 57925889-57926354 57926098-57926354 AAAGCAAGCCAT AAAGCAAGGTGC skip GCAGTTTGGTCA ACCAGCTATATG GCTC (1097) AAAC (1098) 740 chr4: chr4: TACTGATCATAT AAGAGTGCCAAA 2 5 1.00 2.55E−03 exon Mel. 48853992-48862741 48859382-48862741 TGTCCAAGTCAA AAAAGAAGTCAA skip AGTAAACAAGTA AGTAAACAAGTA TGGA (1099) TGGA (1100) 741 chr2: chr2: TGTCATCCATTG TGTCATCCATTG 1 3 1.00 2.77E−02 3′ss Mel. 27604588-27604992 27604672-27604992 TGGAAGAGCCCC TGGAAGAGCTGC GAAACACAGCAG TGGATCAGTGCC AGCT (1101) TGGC (1102) 742 chr6: chr6: TACCGGAAACCT GCTGCCAAAGCC 1 3 1.00 4.97E−02 5′ss Mel. 133136363-133137599 133136227-133137599 AGGAAAAGGCGC TTAGACAAGCGC CAAGCCCATCTT CAAGCCCATCTT TGTG (1103) TGTG (1104) 743 chr12: chr12: GGGTGCAAAAGA GGGTGCAAAAGA 0 1 1.00 8.93E−03 3′ss Mel. 57032980-57033763 57033091-57033763 TCCTGCAGCCAT TCCTGCAGGACT TCCAGGTTGCTG ACAAATCCCTCC AGGT (283) AGGA (284) 744 chr14: chr14: AGGATATCGGTT AGGATATCGGTT 0 1 1.00 1.46E−02 3′ss Mel. 50044571-50052667 50050393-50052667 TCATTAAGAAAG TCATTAAGTTGG ACCTGAGCTGTC ACTAAATGCTCT TTCC (1105) TCCT (1106) 745 chr16: chr16: GCGGCGGGCAGT GCGGCGGGCAGT 0 1 1.00 1.39E−02 3′ss Mel. 85833358-85834789 85833358-85834810 GGCGGCAGGTGT GGCGGCAGAATG ACATTTTTATCT TTGGCTACCAGG TTCA (1107) GTAT (1108) 746 chr19: chr19: TATCCAGCACTG CCTGATTCTCCC 0 1 1.00 3.56E−02 exon Mel. 35647877-35648323 35646514-35648323 ACCACATGGACA CACCAGAGGACA incl. GACGTTGAAAGA GACGTTGAAAGA TACC (1109) TACC (1110) 747 chr21: chr21: TTCATCATGGTG TTCATCATGGTG 0 1 1.00 1.84E−02 3′ss Mel. 27254101-27264033 27254082-27264033 TGGTGGAGCTCT TGGTGGAGGTTG CCTCTTGTTTTT ACGCCGCTGTCA CAGG (1111) CCCC (1112) 748 chr21: chr21: TGAAATCAGAAA TGAAATCAGAAA 0 1 1.00 3.04E−02 3′ss Mel. 46271557-46275124 46271542-46275124 AAAATATGTTTA AAAATATGGCCT TTTTGTTTCAGG GTTTAAAGAAGA CCTG (1113) AAAC (1114) 749 chr3: chr3: CAACGAGAACAA CAACGAGAACAA 0 1 1.00 4.76E−04 3′ss Mel. 101401353-101401614 101401336-101401614 GCTATCAGTTAC GCTATCAGGGCT TTTTACCCCACA GCTAAGGAAGCA GGGC (297) AAAA (298) 750 chr4: chr4: CCATGGTCAAAA CCATGGTCAAAA 0 1 1.00 4.92E−05 3′ss Mel. 152022314-152024139 152022314-152024022 AATGGCAGCACC AATGGCAGACAA AACAGGTCCGCC TGATTGAAGCTC AAAT (344) ACGT (345) 751 chr9: chr9: GCAAGGATATAT GCAAGGATATAT 0 1 1.00 4.68E−04 3′ss Mel. 86593213-86593287 86593194-86593287 AATAACTGCTGC AATAACTGATTG TTTATTTTTCCA GTGTGCCCGTTT CAGA (1115) AATA (1116) 752 chr4: chr4: GAACTGCAAAGG AGTGAATGTAGT 27 54 0.97 4.49E−02 exon Mel. 169911479-169919352 169911479-169923221 CTTCAGAGGATT TGCACCAGGATT incl. TGTACACACAGA TGTACACACAGA TATG (1117) TATG (1038) 753 chrX: chrX: TTGGAGATCAGG GATCTGGATTCT 21 42 0.97 2.52E−02 5′ss Mel. 102940188-102942916 102940188-102941558 ACGCAAAGGTCA CGTTTCAGGTCA CCATCAGAAAAG CCATCAGAAAAG CTAA (1118) CTAA (1119) 754 chr5: chr5: TGGAAGAGGCTA TGGAAGAGGCTA 13 26 0.95 2.18E−02 exon Mel. 137503767-137504910 137504377-137504910 CCTCTGGGGTCA CCTCTGGGGTAA skip ATGAGAGTGAAA CCCCCGGGACTT TGGC (1120) TGCC (1121) 755 chr13: chr13: TCTGGAGCCATA TCTGGAGCCATA 11 22 0.94 4.45E−02 exon Mel. 114291015-114294434 114291015-114292132 CGTGACAGTGAC CGTGACAGAAAT skip CTGACCAACGGT GGCTCAGGGAAC GCAG (1122) TGTT (1123) 756 chr16: chr16: CATCAAGCAGCT CATCAAGCAGCT 11 22 0.94 4.68E−04 3′ss Mel. 57473207-57474683 57473246-57474683 GTTGCAATGTTT GTTGCAATCTGC AGTCCCAGGAAG CCACAAAGAATC CACC (822) CAGC (823) 757 chr22: chr22: CTGCAGTATCTG CTGCAGTATCTG 28 52 0.87 1.79E−02 3′ss Mel. 31724845-31731677 31724910-31731677 TAACCGAGGTCT TAACCGAGGTTT CCAGGCACCAGG CTCCTCTGCCTC AGCC (1124) CTAC (1125) 758 chrX: chrX: ACTAATCTTCAG CAAACACCTCTT 14 26 0.85 1.55E−02 exon Mel. 123224814-123227867 123224614-123227867 CATGCCATTCGG GATTATAATCGG incl. CGTGGCACAAGC CGTGGCACAAGC CTAA (456) CTAA (457) 759 chr7: chr7: TGATTTCAAGTT TGATGAGACTCC 56 100 0.83 5.42E−03 exon Mel. 5028808-5036240 5035213-5036240 TGAACAAGGGGT AGACAGAGGGGT skip TGGCATCTGCAC TGGCATCTGCAC ATCC (1126) ATCC (1127) 760 chr8: chr8: AGCGAGCTCCTC CCGGGGATTGCC 29 52 0.82 4.95E−02 5′ss Mel. 146076780-146078756 146076780-146078377 AGCCTCAGGCAT GGCGCCAGGCAT CTGCATCTGGGA CTGCATCTGGGA CCGA (1128) CCGA (1129) 761 chr5: chr5: AGTTTCTACTAG AGTTTCTACTAG 7 13 0.81 3.69E−03 exon Mel. 139909381-139916922 139909381-139914946 TCCAGTTGGTGA TCCAGTTGGGTT skip CTCTCCTATTCC ACCATCCATTGA ATCT (1130) CCCA (1131) 762 chr1: chr1: CATAGTGGAAGT CATAGTGGAAGT 42 69 0.70 1.02E−05 3′ss Mel. 67890660-67890765 67890642-67890765 GATAGATCTTCT GATAGATCTGGC TTTTCACATTAC CTGAAGCACGAG AGTG (444) GACA (445) 763 chr22: chr22: GGAAAGGACAGC TGAGGTGCCCTA 40 65 0.69 3.49E−02 exon Mel. 42557364-42564614 42557364-42565852 AAGCACAGGTGA AGCACAAGGTGA incl. GACTGTGGAGAT GACTGTGGAGAT GAGA (1132) GAGA (1133) 764 chr6: chr6: AGTTGCATGTTG AGTTGCATGTTG 4 7 0.68 3.75E−03 exon Mel. 30587766-30592659 30587766-30590608 ACTTTAGGGAGT ACTTTAGGAACG skip CTGTGTGAAGCA TGAAGCTCTTGG GCAC (1134) AGCA (1135) 765 chr19: chr19: CCGCCCCCGTTC CCGCCCCCGTTC 41 65 0.65 1.89E−02 3′ss Mel. 2112966-2113334 2112930-2113334 CATCCACGGGGG CATCCACGGACG AGCTCAGTGTGA AGTGTGAGGACG ACAC (1136) CCAA (1137) 766 chr16: chr16: TGGAGCCGAACA TGGAGCCGAACA 8 13 0.64 4.20E−03 3′ss Mel. 89960266-89961490 89960266-89961445 ACATCGTGCTCA ACATCGTGGTTC GCGATGCCTGCC TGCTCCAGACGA GCTT (1138) GCCC (1139) 767 chr10: chr10: TGACGTTCTCTG TGACGTTCTCTG 47 73 0.62 1.42E−03 3′ss Mel. 75554088-75554298 75554088-75554313 TGCTCCAGTGGT TGCTCCAGGTTC TTCTCCCACAGG CCGGCCCCCAAG TTCC (466) TCGC (467) 768 chr12: chr12: GCCTGGAAAGCT GCCTGGAAAGCT 28 42 0.57 1.37E−03 3′ss Mel. 6675490-6675694 6675502-6675694 ACCAAAAGGAGC ACCAAAAGGGAT TGTCCAGACAGC CTCTGCAGGAGC TGGT (1140) TGTC (1141) 769 chr11: chr11: TGTTATTGTAGA TGTTATTGTAGA 37 55 0.56 4.34E−05 3′ss Mel. 85693031-85694908 85693046-85694908 TTCTGGGGGTGG TTCTGGGGGCTT ACTTCTCAAACC TGATGAACTAGG AACA (1142) TGGA (1143) 770 chr2: chr2: GGGGACCAAGAA GGGGACCAAGAA 59 86 0.54 2.26E−02 exon Mel. 55530288-55535944 55529208-55535944 AAGCAGCATGGT AAGCAGCACCAT incl. TGCACTGAAAAG GAATGACCTGGT ACTG (1144) GCAG (1145) 771 chr12: chr12: CAAAAAAGACCA CAAAAAAGACCA 13 19 0.51 2.94E−02 3′ss Mel. 7043741-7044712 7043741-7044709 AAACTGAGGAAC AAACTGAGCAGG TCCCTCGGCCAC AACTCCCTCGGC AGTC (1146) CACA (1147) 772 chr1: chr1: CCAAAGCAGAGA CCAAAGCAGAGA 9 13 0.49 3.58E−02 3′ss Mel. 40209596-40211085 40209596-40211046 CCCAGGAGGTGT CCCAGGAGGGAG ACATGGACATCA AGCCCATTGCTA AGAT (1148) AAAA (1149) 773 chr4: chr4: ACTGGGCTTCCA ACTGGGCTTCCA 63 86 0.44 9.76E−04 exon Mel. 54266006-54280781 54266006-54292038 CCGAGCAGAAAC CCGAGCAGGAGA incl. AGCACTTCTTCT TTACCTGGGGCA CAGT (848) ATTG (849) 774 chr20: chr20: TGCCTAAGGCGG TGCCTAAGGCGG 61 83 0.44 3.34E−02 3′ss Mel. 30310151-30310420 30310133-30310420 ATTTGAATCTCT ATTTGAATAATC TTCTCTCCCTTC TTATCTTGGCTT AGAA (479) TGGA (480) 775 chr4: chr4: GCCGAATCACCT ACTGGGCTTCCA 63 84 0.41 3.70E−03 exon Mel. 54280889-54292038 54266006-54292038 GATCTAAGGAGA CCGAGCAGGAGA incl. TTACCTGGGGCA TTACCTGGGGCA ATTG (1150) ATTG (849) 776 chr1: chr1: ACGCCGCAAGTC AGCACCCATGGG 66 87 0.39 2.24E−02 exon Mel. 47024472-47025905 47024472-47027149 CTCCAGAGGAAC TGCAGGGGGAAC incl. AGCAGCACAATG AGCAGCACAATG GACC (1151) GACC (1152) 777 chr1: chr1: AACCAGTAACAA AACCAGTAACAA 59 76 0.36 1.42E−02 3′ss Mel. 150249040-150252050 150249040-150252053 CGGAACCTCAGA CGGAACCTAGTC GTCCAGATCTGA CAGATCTGAACG ACGA (1153) ATGC (1154) 778 chr20: chr20: GAGACCGCGTGC GAGACCGCGTGC 70 90 0.36 3.80E−03 3′ss Mel. 62577996-62587612 62577993-62587612 GAGGACCGCAGC GAGGACCGCAAT AATGCAGAGTCC GCAGAGTCCCTG CTGG (1155) GACA (1156) 779 chr1: chr1: GTCTCTGGCAAG GTCTCTGGCAAG 78 100 0.35 3.86E−02 3′ss Mel. 211836994-211840447 211836970-211840447 TAATCCAGAACT TAATCCAGTAAT TCTTAATCTTCC TAAGAAGAAAGT ATCC (1157) TCAT (1158) 780 chr3: chr3: AAGCATGTAGAA AAGCATGTAGAA 44 56 0.34 4.73E−02 3′ss Mel. 133305566-133306002 133305566-133306739 AGCCGGAACAGG AGCCGGAAGGAT TACTTAAAATGA AAAGAAATGGAG ATGC (1159) AAGA (1160) 781 chr1: chr1: AGCACCCATGGG AGCACCCATGGG 69 87 0.33 4.36E−02 exon Mel. 47025949-47027149 47024472-47027149 TGCAGGGGCAAG TGCAGGGGGAAC incl. CTCCAGAAAAGG AGCAGCACAATG GACT (1161) GACC (1152) 782 chr1: chr1: TCCACAAGAGCG AGGCGGTGAGTG 46 58 0.33 4.32E−02 5′ss Mel. 17330906-17331201 17330906-17331186 AGGAGGCGAAGC TCGGACAGAAGC GGGTGCTGCGGT GGGTGCTGCGGT ATTA (1162) ATTA (1163) 783 chr1: chr1: TCCGCCCCACAG GGCGGAGACATG 74 91 0.29 8.93E−03 5′ss Mel. 155917806-155920089 155917806-155920059 TCCACGAGACTT GACCAGAGACTT TACCAGAATGCA TACCAGAATGCA GGAC (1164) GGAC (1165) 784 chr17: chr17: TTGATCTTCGGC TTGATCTTCGGC 72 84 0.22 4.78E−02 3′ss Mel. 38080478-38083736 38080473-38083736 CCCACACGAACA CCCACACGCAGA GCAGAGAGGGGC GAGGGGCAGCAG AGCA (1166) GATG (1167) 785 chr2: chr2: GAAAAACTTTCC GAAAAACTTTCC 81 94 0.21 4.90E−02 3′ss Mel. 242590750-242592926 242590750-242592721 AGCCATTGGGGG AGCCATTGGAGG GACAGGCCCCAC TTGTCGGGACAT CTCG (1168) TTCA (1169) 786 chr9: chr9: GCGCTCGCCCGG CCGCAGGATACC 76 86 0.18 2.12E−02 5′ss Mel. 37422830-37424841 37422802-37424841 GCGGCAGACTGT CGCCGAGGCTGT GAGGTGGAGCAG GAGGTGGAGCAG TGGG (1170) TGGG (1171) 787 chr20: chr20: CGGGACGACTTC GCAGCATCTGCC 78 86 0.14 3.03E−02 exon Mel. 32661672-32663679 32661441-32663679 TACGACAGGCTC ATATACAGGCTC incl. TTCGACTACCGG TTCGACTACCGG GGCC (1172) GGCC (1173) 788 chr3: chr3: ACTGAAGCAGCA ACTGAAGCAGCA 92 98 0.09 3.80E−03 3′ss Mel. 184084588-184085964 184084588-184085900 ACACGCCTCTCT ACACGCCTGCTG GCGTACGTGTCC AGATTGAGAGCT TATG (1174) GCTG (1175) 789 chr19: chr19: CTGCCGGCGGAG CTGCCGGCGGAG 93 99 0.09 7.19E−03 3′ss Mel. 58817582-58823531 58817582-58823562 AATATAAGGAGA AATATAAGGTGT TGGACAAACCGT GTGTGACCATGG GTGG (1176) AACG (1177) 790 chr5: chr5: CAACCTCTAAGA CAACCTCTAAGA 97 99 0.03 2.75E−02 3′ss Mel. 179225591-179225927 179225576-179225927 CTGGAGCGGTTC CTGGAGCGTGGG TTCTTCCGCAGT AACATCGAGCAC GGGA (1178) CCGG (1179)

Certain splice variants are associated with more than one disease, and thus appear in Table 1 more than one time. In certain instances, splice variants associated with more than one cancer type may have different expression levels in each disease, so there may be more than one set of expression data for a given splice variant. Variants differentially expressed across all tested cancer types can be used to evaluate cells having SF3B1 neomorphic mutations in additional cancer types. Such variants are shown in the following rows of Table 1 (triplicates represent the same splice junction, measured in different cancer types): [13, 272, 525], [27, 286, 527], [33, 536, 330], [107, 445, 657], [28, 350, 573], [229, 762, 467], [240, 508, 767], [7, 356, 524], [76, 374, 596], [35, 547, 280], [84, 364, 571], [85, 564, 297], [24, 597, 296], [21, 372, 545], [36, 576, 407], [105, 423, 639], [62, 580, 447], [31, 279, 528], [235, 758, 439], [306, 89, 666], [34, 295, 533], [390, 72, 640], [48, 343, 554], [360, 65, 540], [178, 329, 750], [71, 265, 556], [15, 283, 530], [18, 267, 583], [129, 418, 622], [333, 25, 541], [247, 500, 774], [259, 5, 542], [152, 438, 615], [292, 1, 517], [81, 543, 443], [347, 70, 592], [91, 431, 617], [30, 298, 582], [17, 334, 602], [16, 276, 559], [51, 426, 548], [118, 401, 566], [83, 435, 574], and [269, 45, 546]. In certain embodiments, variants that are nonspecific to a particular cancer type can be chosen from the following rows of Table 1: [13, 272, 525], [27, 286, 527], [33, 536, 330], [107, 445, 657], [28, 350, 573], [240, 508, 767], [7, 356, 524], [84, 364, 571], [24, 597, 296], [21, 372, 545], [105, 423, 639], [62, 580, 447], [31, 279, 528], [235, 758, 439], [306, 89, 666], [34, 295, 533], [390, 72, 640], [360, 65, 540], [178, 329, 750], [71, 265, 556], [15, 283, 530], [18, 267, 583], [247, 500, 774], [152, 438, 615], [292, 1, 517], [81, 543, 443], [91, 431, 617], [30, 298, 582], [16, 276, 559], or [51, 426, 548].

Certain embodiments of the invention provide splice variants as markers for cancer. In certain circumstances, cancer cells with a neomorphic SF3B1 protein demonstrate differential expression of certain splice variants compared to cells without a neomorphic SF3B1 protein. The differential expression of one or more splice variants therefore may be used to determine whether a patient has cancer with a neomorphic SF3B1 mutation. In certain embodiments, the patient is also determined to have a cancer cell having a mutant SF3B1 protein. In these methods, one or more of the splice variants listed in Table 1 can be measured to determine whether a patient has cancer with a neomorphic SF3B1 mutation. In certain embodiments, one or more aberrant splice variants from Table 1 are measured. In other embodiments, one or more canonical splice variants are measured. Sometimes, both aberrant and canonical variants are measured.

In some embodiments, one or more aberrant splice variants selected from rows 260, 262, 263, 265, 266, 267, 272, 273, 275, 276, 277, 279, 281, 282, 286, 287, 288, 290, 294, 295, 296, 298, 299, 301, 302, 304, 305, 306, 308, 310, 312, 313, 315, 316, 318, 320, 321, 322, 323, 324, 325, 326, 327, 328, 329, 330, 331, 335, 337, 339, 342, 346, 348, 349, 350, 352, 353, 354, 355, 356, 357, 358, 362, 363, 365, 366, 368, 369, 370, 372, 375, 377, 378, 379, 380, 381, 382, 383, 384, 387, 388, 389, 390, 391, 392, 393, 394, 397, 398, 400, 402, 403, 404, 405, 406, 413, 415, 416, 417, 419, 420, 421, 424, 425, 428, 429, 430, 431, 432, 433, 436, 437, 438, 439, 440, 441, 442, 443, 444, 445, 446, 447, 448, 449, 450, 451, 452, 454, 455, 456, 458, 459, 460, 461, 462, 464, 465, 468, 469, 471, 472, 473, 474, 475, 476, 477, 478, 480, 481, 483, 484, 485, 486, 487, 488, 490, 491, 494, 496, 497, 498, 500, 501, 502, 503, 504, 505, 506, 507, 508, 509, 510, 511, 513, 514, 515, or 516 of Table 1 can be measured in a patient suspected of having CLL. In additional embodiments, a patient suspected of having CLL can be identified by measuring the amounts of one or more of the following aberrant splice variants listed in Table 1: row 259, 269, 270, 271, 274, 278, 280, 282, 292, 296, 297, 302, 306, 330, 331, 333, 343, 347, 355, 360, 361, 371, 373, 376, 378, 390, 391, 407, 408, 423, 424, 425, 433, 434, 439, 443, 447, 448, 451, 452, 453, 458, 459, 460, 462, 463, 466, 467, 468, 469, 470, 472, 479, 482, or 489. In additional embodiments, a patient suspected of having CLL can be identified by measuring the amounts of one or more of the following aberrant splice variants listed in Table 1: row 282, 292, 296, 302, 306, 330, 331, 343, 355, 360, 373, 378, 390, 391, 423, 424, 425, 433, 434, 439, 443, 447, 448, 451, 452, 458, 459, 460, 462, 463, 466, 468, 469, 470, 472, 479, 482, or 489. In still further embodiments, a patient suspected of having CLL can be identified by measuring the amount of one or more of the following aberrant splice variants listed in Table 1: row 282, 296, 302, 306, 330, 331, 355, 378, 390, 391, 424, 425, 433, 439, 443, 447, 448, 451, 452, 458, 459, 460, 462, 468, 469, or 472.

In other embodiments, one or more aberrant splice variants selected from rows 2, 3, 4, 7, 9, 10, 11, 13, 16, 18, 19, 20, 21, 22, 23, 24, 27, 28, 30, 31, 32, 33, 34, 37, 38, 39, 40, 41, 42, 43, 46, 47, 49, 50, 52, 53, 54, 56, 57, 58, 61, 62, 63, 64, 66, 67, 68, 71, 72, 75, 77, 78, 79, 80, 81, 82, 84, 87, 88, 89, 90, 91, 92, 94, 95, 97, 98, 99, 100, 101, 103, 104, 106, 107, 108, 109, 110, 111, 112, 113, 114, 116, 117, 119, 120, 121, 122, 123, 124, 125, 126, 127, 131, 132, 133, 134, 135, 136, 138, 139, 140, 141, 142, 143, 144, 146, 147, 150, 152, 154, 155, 156, 157, 159, 163, 164, 165, 167, 168, 169, 170, 171, 172, 173, 174, 175, 176, 177, 178, 179, 180, 181, 182, 183, 185, 186, 187, 188, 189, 190, 191, 192, 193, 194, 195, 196, 197, 198, 199, 200, 201, 202, 203, 204, 205, 206, 207, 208, 209, 210, 211, 212, 213, 214, 215, 216, 217, 218, 219, 220, 221, 222, 223, 224, 225, 226, 227, 228, 230, 231, 232, 233, 235, 236, 237, 238, 239, 240, 241, 242, 243, 244, 247, 249, 250, 251, 252, 253, 254, 255, 256, or 257 of Table 1 can be measured in a patient suspected of having breast cancer. In additional embodiments, a patient suspected of having breast cancer can be identified by measuring the amounts of one or more of the following aberrant splice variants listed in Table 1: row 7, 8, 9, 10, 26, 48, 66, 105, 121, 135, 136, or 166. In additional embodiments, a patient suspected of having breast cancer can be identified by measuring the amounts of one or more of the following aberrant splice variants listed in Table 1: row 7, 8, 9, 10, 26, 48, 66, 105, 121, 135, or 136. In still further embodiments, a patient suspected of having breast cancer can be identified by measuring the amount of one or more of the following aberrant splice variants listed in Table 1: row 7, 9, 10, 66, 121, 135, or 136.

In further embodiments, one or more aberrant splice variants selected from rows 518, 519, 520, 521, 523, 524, 525, 526, 527, 528, 529, 531, 533, 534, 536, 537, 538, 539, 543, 544, 545, 549, 551, 552, 553, 555, 556, 557, 558, 559, 560, 561, 562, 563, 565, 567, 568, 569, 570, 572, 573, 575, 577, 578, 579, 580, 581, 582, 583, 584, 585, 588, 589, 590, 591, 593, 595, 597, 598, 599, 600, 601, 603, 604, 605, 606, 607, 608, 609, 610, 611, 612, 613, 614, 615, 616, 617, 618, 619, 620, 621, 623, 625, 627, 628, 629, 630, 632, 634, 635, 636, 637, 638, 640, 641, 643, 644, 645, 646, 647, 648, 649, 650, 651, 652, 654, 657, 658, 659, 661, 662, 663, 664, 665, 666, 667, 668, 669, 670, 671, 672, 673, 674, 675, 676, 677, 678, 680, 682, 683, 684, 685, 686, 687, 688, 689, 690, 692, 694, 696, 697, 698, 699, 700, 701, 702, 703, 705, 706, 707, 708, 709, 710, 711, 712, 713, 714, 715, 716, 717, 718, 719, 720, 721, 722, 723, 724, 725, 726, 727, 728, 730, 731, 732, 733, 734, 735, 736, 737, 738, 739, 740, 741, 742, 743, 744, 745, 746, 747, 748, 750, 751, 752, 753, 754, 755, 756, 757, 758, 759, 760, 763, 764, 765, 766, 767, 768, 770, 771, 772, 773, 774, 775, 776, 777, 778, 779, 780, 781, 782, 783, 784, 785, 786, 787, 788, 789, or 790 of Table 1 can be measured in a patient suspected of having melanoma. In additional embodiments, a patient suspected of having melanoma can be identified by measuring the amounts of one or more of the following aberrant splice variants listed in Table 1: row 519, 521, 522, 535, 554, 587, 594, 601, 618, 639, 654, 655, 670, 679, 680, 727, 729, or 730. In additional embodiments, a patient suspected of having melanoma can be identified by measuring the amounts of one or more of the following aberrant splice variants listed in Table 1: row 519, 521, 522, 535, 554, 587, 601, 618, 639, 654, 670, 680, 727, or 730. In still further embodiments, a patient suspected of having melanoma can be identified by measuring the amount of one or more of the following aberrant splice variants listed in Table 1: row 519, 521, 601, 618, 654, 670, 680, 727, or 730.

In some embodiments, one or more of the aberrant variants are selected from rows 21, 31, 51, 81, 118, 279, 372, 401, 426, 443, 528, 543, 545, 548 or 566 of Table 1. In certain embodiments, a patient suspected of having cancer can be identified by measuring the amount of one or more of the aberrant variants selected from 21, 31, 51, 81, 118, 279, 372, 401, 426, 443, 528, 543, 545, 548 or 566. In various embodiments the cancer may be CLL, breast cancer, or melanoma, for example.

Additional methods include predicting or monitoring the efficacy of a treatment for cancer by measuring the level of one or more aberrant splice variants in samples obtained from patients before or during the treatment. For example, a decrease in the levels of one or more aberrant splice variants over the course of treatment may indicate that the treatment is effective. In other cases, the absence of a decrease or an increase in the levels of one or more aberrant splice variants over the course of treatment may indicate that the treatment is not effective and should be adjusted, supplemented, or terminated. In some embodiments, the splice variants are used to track and adjust individual patient treatment effectiveness.

Embodiments of the invention also encompass methods of stratifying cancer patients into different categories based on the presence or absence of one or more particular splice variants in patient samples or the detection of one or more particular splice variants at levels that are elevated or reduced relative to those in normal cell samples. Categories may be different prognostic categories, categories of patients with varying rates of recurrence, categories of patients that respond to treatment and those that do not, and categories of patients that may have particular negative side effects, and the like. According to the categories in which individual patients fall, optimal treatments may then be selected for those patients, or particular patients may be selected for clinical trials.

Embodiments also encompass methods of distinguishing cancerous cells with SF3B1 neomorphic mutations from normal cells by using the splice variants disclosed herein as markers. Such methods may be employed, for example, to assess the growth or loss of cancerous cells and to identify cancerous cells to be treated or removed. In some embodiments, the splice variants are measured in cancerous tissue having cells with a neomorphic SF3B1 mutation before and after anti-cancer treatment, for the purpose of monitoring the effect of the treatment on cancer progression.

In additional embodiments, administering an SF3B1 modulator to a cell, such as a cancer cell, can alter the differential expression of splice variants. Accordingly, the change in expression of one or more splice variants can be used to evaluate the effect of the SF3B1 modulator on the SF3B1 protein. In one embodiment, the effect of an SF3B1 modulator on a CLL cell is evaluated by applying an SF3B1 modulator to such a cell, then detecting or quantifying one or more of the splice variants in Table 1. In additional embodiments the one or more splice variants are chosen from rows 258-516 of Table 1. In further embodiments, the one or more splice variants are chosen from rows 260, 262, 263, 265, 266, 267, 272, 273, 275, 276, 277, 279, 281, 282, 286, 287, 288, 290, 294, 295, 296, 298, 299, 301, 302, 304, 305, 306, 308, 310, 312, 313, 315, 316, 318, 320, 321, 322, 323, 324, 325, 326, 327, 328, 329, 330, 331, 335, 337, 339, 342, 346, 348, 349, 350, 352, 353, 354, 355, 356, 357, 358, 362, 363, 365, 366, 368, 369, 370, 372, 375, 377, 378, 379, 380, 381, 382, 383, 384, 387, 388, 389, 390, 391, 392, 393, 394, 397, 398, 400, 402, 403, 404, 405, 406, 413, 415, 416, 417, 419, 420, 421, 424, 425, 428, 429, 430, 431, 432, 433, 436, 437, 438, 439, 440, 441, 442, 443, 444, 445, 446, 447, 448, 449, 450, 451, 452, 454, 455, 456, 458, 459, 460, 461, 462, 464, 465, 468, 469, 471, 472, 473, 474, 475, 476, 477, 478, 480, 481, 483, 484, 485, 486, 487, 488, 490, 491, 494, 496, 497, 498, 500, 501, 502, 503, 504, 505, 506, 507, 508, 509, 510, 511, 513, 514, 515, or 516 of Table 1. In further embodiments, the one or more splice variants are chosen from rows 259, 269, 270, 271, 274, 278, 280, 282, 292, 296, 297, 302, 306, 330, 331, 333, 343, 347, 355, 360, 361, 371, 373, 376, 378, 390, 391, 407, 408, 423, 424, 425, 433, 434, 439, 443, 447, 448, 451, 452, 453, 458, 459, 460, 462, 463, 466, 467, 468, 469, 470, 472, 479, 482, or 489. In additional embodiments, the one or more splice variants are chosen from rows 282, 292, 296, 302, 306, 330, 331, 343, 355, 360, 373, 378, 390, 391, 423, 424, 425, 433, 434, 439, 443, 447, 448, 451, 452, 458, 459, 460, 462, 463, 466, 468, 469, 470, 472, 479, 482, or 489 of Table 1. In still further embodiments, the one or more splice variants are chosen from rows 282, 296, 302, 306, 330, 331, 355, 378, 390, 391, 424, 425, 433, 439, 443, 447, 448, 451, 452, 458, 459, 460, 462, 468, 469, or 472 of Table 1.

In certain embodiments, the effect of an SF3B1 modulator on a breast cancer cell is evaluated by applying an SF3B1 modulator to such a cell, then detecting or quantifying one or more of the splice variants in Table 1. In additional embodiments the one or more splice variants are chosen from rows 1-257 of Table 1. In further embodiments, the one or more splice variants are chosen from rows 2, 3, 4, 7, 9, 10, 11, 13, 16, 18, 19, 20, 21, 22, 23, 24, 27, 28, 30, 31, 32, 33, 34, 37, 38, 39, 40, 41, 42, 43, 46, 47, 49, 50, 52, 53, 54, 56, 57, 58, 61, 62, 63, 64, 66, 67, 68, 71, 72, 75, 77, 78, 79, 80, 81, 82, 84, 87, 88, 89, 90, 91, 92, 94, 95, 97, 98, 99, 100, 101, 103, 104, 106, 107, 108, 109, 110, 111, 112, 113, 114, 116, 117, 119, 120, 121, 122, 123, 124, 125, 126, 127, 131, 132, 133, 134, 135, 136, 138, 139, 140, 141, 142, 143, 144, 146, 147, 150, 152, 154, 155, 156, 157, 159, 163, 164, 165, 167, 168, 169, 170, 171, 172, 173, 174, 175, 176, 177, 178, 179, 180, 181, 182, 183, 185, 186, 187, 188, 189, 190, 191, 192, 193, 194, 195, 196, 197, 198, 199, 200, 201, 202, 203, 204, 205, 206, 207, 208, 209, 210, 211, 212, 213, 214, 215, 216, 217, 218, 219, 220, 221, 222, 223, 224, 225, 226, 227, 228, 230, 231, 232, 233, 235, 236, 237, 238, 239, 240, 241, 242, 243, 244, 247, 249, 250, 251, 252, 253, 254, 255, 256, or 257 of Table 1. In additional embodiments, the one or more splice variants are chosen from rows 7, 8, 9, 10, 26, 48, 66, 105, 121, 135, 136, or 166 of Table 1. In further embodiments, the one or more splice variants are chosen from rows 7, 8, 9, 10, 26, 48, 66, 105, 121, 135, or 136 of Table 1. In still further embodiments, the one or more splice variants are chosen from rows 7, 9, 10, 66, 121, 135, or 136 of Table 1.

In a further embodiment, the effect of an SF3B1 modulator on a melanoma cell is evaluated by applying an SF3B1 modulator to such a cell, then detecting or quantifying one or more of the splice variants in Table 1. In additional embodiments the one or more splice variants are chosen from rows 517-790 of Table 1. In further embodiments, the one or more splice variants are chosen from rows 518, 519, 520, 521, 523, 524, 525, 526, 527, 528, 529, 531, 533, 534, 536, 537, 538, 539, 543, 544, 545, 549, 551, 552, 553, 555, 556, 557, 558, 559, 560, 561, 562, 563, 565, 567, 568, 569, 570, 572, 573, 575, 577, 578, 579, 580, 581, 582, 583, 584, 585, 588, 589, 590, 591, 593, 595, 597, 598, 599, 600, 601, 603, 604, 605, 606, 607, 608, 609, 610, 611, 612, 613, 614, 615, 616, 617, 618, 619, 620, 621, 623, 625, 627, 628, 629, 630, 632, 634, 635, 636, 637, 638, 640, 641, 643, 644, 645, 646, 647, 648, 649, 650, 651, 652, 654, 657, 658, 659, 661, 662, 663, 664, 665, 666, 667, 668, 669, 670, 671, 672, 673, 674, 675, 676, 677, 678, 680, 682, 683, 684, 685, 686, 687, 688, 689, 690, 692, 694, 696, 697, 698, 699, 700, 701, 702, 703, 705, 706, 707, 708, 709, 710, 711, 712, 713, 714, 715, 716, 717, 718, 719, 720, 721, 722, 723, 724, 725, 726, 727, 728, 730, 731, 732, 733, 734, 735, 736, 737, 738, 739, 740, 741, 742, 743, 744, 745, 746, 747, 748, 750, 751, 752, 753, 754, 755, 756, 757, 758, 759, 760, 763, 764, 765, 766, 767, 768, 770, 771, 772, 773, 774, 775, 776, 777, 778, 779, 780, 781, 782, 783, 784, 785, 786, 787, 788, 789, or 790 of Table 1. In still further embodiments, the one or more splice variants are chosen from rows 519, 521, 522, 535, 554, 587, 594, 601, 618, 639, 654, 655, 670, 679, 680, 727, 729, or 730 of Table 1. In additional embodiments, the one or more splice variants are chosen from rows 519, 521, 522, 535, 554, 587, 601, 618, 639, 654, 670, 680, 727, or 730 of Table 1. In still further embodiments, the one or more splice variants are chosen from rows 519, 521, 601, 618, 654, 670, 680, 727, or 730 of Table 1.

In some embodiments, the effect of an SF3B1 modulator on a cancer cell is evaluated by applying an SF3B1 modulator to such a cell, then detecting or quantifying one or more of the aberrant variants selected from rows 21, 31, 51, 81, 118, 279, 372, 401, 426, 443, 528, 543, 545, 548 or 566 of Table 1. In various embodiments, the cancer cell may be a CLL cell, a breast cancer cell, or a melanoma cell, for example.

The specific splice variants that are useful for demonstrating the effect of an SF3B1 modulator on one type of cancer cell may not be useful for demonstrating an effect of the modulator on another type of cancer cell. Aberrant splice variants that are appropriate for revealing such effects in particular cancer cells will be apparent from the description and examples provided herein.

In some embodiments, aberrant splice variants that are present at elevated levels in a cell having a neomorphic SF3B1 protein are used as markers. In other embodiments, splice variants that have reduced levels in a cell having a neomorphic SF3B1 protein are used as markers. In some embodiments, more than one splice variant will be measured. When more than one splice variant is used, they may all have elevated levels, all have reduced levels, or a mixture of splice variants with elevated and reduced levels may be used. In certain embodiments of the methods described herein, more than one aberrant splice variant is measured. In other embodiments, at least one aberrant and at least one canonical splice variant is measured. In some cases, both an aberrant and canonical splice variant associated with a particular genomic location will be measured. In other circumstances, a measured canonical splice variant will be at a different genomic location from the measured aberrant splice variant(s).

Before performing an assay for splice variants in a cell, one may determine whether the cell has a mutant SF3B1 protein. In certain embodiments, the assay for splice variants is performed if the cell has been determined to have a neomorphic SF3B1 mutant protein.

Samples

Cell samples can be obtained from a variety of biological sources. Exemplary cell samples include but are not limited to a cell culture, a cell line, a tissue, oral tissue, gastrointestinal tissue, an organ, an organelle, a biological fluid, a blood sample, a urine sample, a skin sample, and the like. Blood samples may be whole blood, partially purified blood, or a fraction of whole or partially purified blood, such as peripheral blood mononucleated cells (PBMCs). The source of a cell sample may be a solid tissue sample such as a tissue biopsy. Tissue biopsy samples may be biopsies from breast tissue, skin, lung, or lymph nodes. Samples may be samples of bone marrow, including bone marrow aspirates and bone marrow biopsies.

In certain embodiments, the cells are human cells. Cells may be cancer cells, for example hematological cancer cells or solid tumor cells. Hematological cancers include chronic lymphocytic leukemia, acute lymphoblastic leukemia, acute myeloid leukemia, chronic myeloid leukemia, chronic myelomonocytic leukemia, acute monocytic leukemia, Hodgkin's lymphoma, Non-Hodgkin's lymphoma, and multiple myeloma. Solid tumors include carcinomas, such as adenocarcinomas, and may be selected from breast, lung, liver, prostate, pancreatic, colon, colorectal, skin, ovarian, uterine, cervical, or renal cancers. Cell samples may be obtained directly from a patient or derived from cells obtained from a patient, such as cultured cells derived from a biological fluid or tissue sample. Samples may be archived samples, such as kryopreserved samples, of cells obtained directly from a subject or of cells derived from cells obtained from a patient.

In certain embodiments, cells are obtained from patients suspected of having cancer. The patients may show signs and symptoms of cancer, such as one or more common symptoms of CLL, which include enlarged lymph nodes, liver, or spleen, higher-than-normal white blood cell counts, recurring infections, loss of appetite or early satiety, abnormal bruising, fatigue, and night sweats. In additional embodiments, the cells have a mutant SF3B1 protein.

Cell samples described herein may be used in any of the methods presently disclosed.

Detection of Splice Variants

Certain embodiments of the methods described herein involve detection or quantification of splice variants. A variety of methods exists for detecting and quantifying nucleic acids, and each may be adapted for detection of splice variants in the described embodiments. Exemplary methods include an assay to quantify nucleic acid such as nucleic acid barcoding, nanoparticle probes, in situ hybridization, microarray, nucleic acid sequencing, and PCR-based methods, including real-time PCR (RT-PCR).

Nucleic acid assays utilizing barcoding technology such as NanoString® assays (NanoString Technologies) may be performed, for example, as described in U.S. Pat. No. 8,519,115; U.S. Pat. No. 7,919,237; and in Kulkarni, M. M., 2011, “Digital Multiplexed Gene Expression Analysis Using the NanoString nCounter System.” Current Protocols in Molecular Biology, 94:25B.10.1-25B.10.17. In an exemplary assay, a pair of probes is used to detect a particular nucleotide sequence of interest, such as a particular splice variant of interest. The probe pair consists of a capture probe and a reporter probe and that each include a sequence of from about 35 to 50 bases in length that is specific for a target sequence. The capture probe includes an affinity label such as biotin at its 3′ end that provides a molecular handle for surface-attachment of target mRNAs for digital detection, and the reporter probe includes a unique color code at its 5′ end that provides molecular barcoding of the hybridized mRNA target sequence. Capture and reporter probe pairs are hybridized to target mRNA in solution, and after excess probes are removed, the target mRNA-probe complexes are immobilized in an nCounter® cartridge. A digital analyzer acquires direct images of the surface of the cartridge to detect color codes corresponding to specific mRNA splice variant sequences. The number of times a color-coded barcode for a particular splice variant is detected reflects the levels of a particular splice variant in the mRNA library. For the detection of splice variants, either the capture or the reporter probe may span a given splice variant's exon-exon or intron-exon junction. In other embodiments, one or both of the capture and reporter probes' target sequences correspond to the terminal sequences of two exons at an exon-exon junction or to the terminal sequences of an intron and an exon at an intron-exon junction, whereby one probe extends to the exon-exon or intron-exon junction, but does not span the junction, and the other probe binds a sequence that begins on opposite side of the junction and extends into the respective exon or intron.

In exemplary PCR-based methods, a particular splice variant may be detected by specifically amplifying a sequence that contains the splice variant. For example, the method may employ a first primer specifically designed to hybridize to a first portion of the splice variant, where the splice variant is a sequence that spans an exon-exon or intron-exon junction at which alternative splicing occurs. The method may further employ a second opposing primer that hybridizes to a segment of the PCR extension product of the first primer that corresponds to another sequence in the gene, such as a sequence at an upstream or downstream location. The PCR detection method may be quantitative (or real-time) PCR. In some embodiments of quantitative PCR, an amplified PCR product is detected using a nucleic acid probe, wherein the probe may contain one or more detectable labels. In certain quantitative PCR methods, the amount of a splice variant of interest is determined by detecting and comparing levels of the splice variant to an appropriate internal control.

Exemplary methods for detecting splice variants using an in situ hybridization assay such as RNAscope® (Advanced Cell Diagnostics) include those described by Wang, F., et al., “RNAscope: a novel in situ RNA analysis platform for formalin-fixed, paraffin-embedded tissues,” J. Mol. Diagn. 2012 January; 14(1):22-9. RNAscope® assays may be used to detect splice variants by designing a pair of probes that targets a given splice variant, and are hybridized to target RNA in fixed and permeabilized cells. Target probes are designed to hybridize as pairs which, when hybridized to the target sequence, create a binding site for a preamplifier nucleic acid. The preamplifier nucleic acid, in turn, harbors multiple binding sites for amplifier nucleic acids, which in turn contain multiple binding sites for a labeled probe carrying a chromogenic or fluorescent molecule. In some embodiments, one of the RNAscope® target probes spans a given splice variant's exon-exon or intron-exon junction. In other embodiments, the target probes' target sequences correspond to the terminal sequences of two exons at an exon-exon junction or to the terminal sequences of an intron and an exon at an intron-exon junction, whereby one probe in the target probe pair extends to the exon-exon or intron-exon junction, but does not span the junction, and the other probe binds a sequence beginning on opposite side of the junction and extending into the respective exon or intron.

Exemplary methods for detecting splice variants using nanoparticle probes such as SmartFlare™ (Millipore) include those described in Seferos et al., “Nano-flares: Probes for Transfection and mRNA Detection in Living Cells,” J. Am. Chem. Soc. 129(50):15477-15479 (2007) and Prigodich, A. E., et al., “Multiplexed Nanoflares: mRNA Detection in Live Cells,” Anal. Chem. 84(4):2062-2066 (2012). SmartFlare™ detection probes may be used to detect splice variants by generating gold nanoparticles that are modified with one or more nucleic acids that include nucleotide recognition sequences that (1) are each complementary to a particular splice variant to be detected and (2) are each hybridized to a complementary fluorophore-labeled reporter nucleic acid. Upon uptake of the probe by a cell, a target splice variant sequence may hybridize to the one or more nucleotide recognition sequences and displace the fluorophore-labeled reporter nucleic acid. The fluorophore-labeled reporter nucleic acid, whose fluorophore had been quenched due to proximity to the gold nanoparticle surface, is then liberated from the gold nanoparticle, and the fluorophore may then be detected when free of the quenching effect of the nanoparticle. In some embodiments, nucleotide recognition sequences in the probes recognize a sequence that spans a given splice variant's exon-exon or intron-exon junction. In some embodiments, nucleotide recognition sequences in the probes recognize a sequence that is only on one side of the splice variant's exon-exon or intron-exon junction, including a sequence that terminates at the junction and a sequence that terminates one or more nucleotides away from the junction.

Exemplary methods for detecting splice variants using nucleic acid sequencing include RNA sequencing (RNA-Seq) described in Ren, S. et al. “RNA-Seq analysis of prostate cancer in the Chinese population identifies recurrent gene fusions, cancer-associated long noncoding RNAs and aberrant alternative splicings.” Cell Res 22, 806-821, doi:10.1038/cr.2012.30 (2012); and van Dijk et al., “Ten years of next-generation sequencing technology.” Trends Genet 30(9):418-26 (2014). In some embodiments, high-throughput sequencing, such as next-generation sequencing (NGS) technologies, may be used to dected splice variants. For example, the method may employ commercial sequencing platforms available for RNA-Seq, such as, e.g., Illumina, SOLID, Ion Torrent, and Roche 454. In some embodiments, the sequencing method may include pyrosequencing. For example, a sample may be mixed with sequencing enzymes and primer and exposed to a flow of one unlabeled nucleotide at a time, allowing synthesis of the complementary DNA strand. When a nucleotide is incorporated, pyrophosphate is released leading to light emission, which is monitored in real time. In some embodiments, the sequencing method may include semiconductor sequencing. For example, proton instead of pyrophosphate may be released during nucleotide incorporation and detected in real time by ion sensors. In some embodiments, the method may include sequencing with reversible terminators. For example, the synthesis reagents may include primers, DNA polymerase, and four differently labelled, reversible terminator nucleotides. After incorporation of a nucleotide, which is identified by its color, the 3′ terminator on the base and the fluorophore are removed, and the cycle is repeated. In some embodiments, the method may include sequencing by ligation. For example, a sequencing primer may be hybridized to an adapter, with the 5′ end of the primer available for ligation to an oligonucleotide hybridizing to the adjacent sequence. A mixture of octamers, in which bases 4 and 5 are encoded by one of four color labels, may compete for ligation to the primer. After color detection, the ligated octamer may be cleaved between position 5 and 6 to remove the label, and the cycle may be repeated. Thereby, in the first round, the process may determine possible identities of bases in positions 4, 5, 9, 10, 14, 15, etc. The process may be repeated, offset by one base using a shorter sequencing primer, to determine positions 3, 4, 8, 9, 13, 14, etc., until the first base in the sequencing primer is reached.

Other nucleic acid detection and analytical methods that also distinguish between splice variants of a given exon-exon or intron-exon junction in a gene by identifying the nucleotide sequence on both sides of the junction may be utilized to detect or quantify the splice variants disclosed herein. For example, splice variants of an exon-exon junction may be detected by primer extension methods in which a primer that binds to one exon is extended into the exon on the other side of the junction according to the sequence of that adjacent exon. See, for example, McCullough, R. M., et al., “High-throughput alternative splicing quantification by primer extension and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry,” Nucleic Acids Research, 2005 Jun. 20; 33(11):e99; and Milani, L., et al., “Detection of alternatively spliced transcripts in leukemia cell lines by minisequencing on microarrays,” Clin. Chem. 52: 202-211 (2006). Detection of variants on a large scale may be performed using expression microarrays that carry exon-exon or intron-exon junction probes, as described, for example, in Johnson, J. M. et al., “Genome-wide survey of human alternative pre-mRNA splicing with exon junction microarrays,” Science 302: 2141-2144 (2003); and Modrek, B., et al., “Genome-wide detection of alternative splicing in expressed sequences of human genes,” Nucleic Acids Res 29: 2850-2859 (2001).

Various embodiments include reagents for detecting splice variants of the invention. In one example, reagents include NanoString® probes designed to measure the amount of one or more of the aberrant splice variants listed in Table 1. Probes for nucleic acid quantification assays such as barcoding (e.g. NanoString®), nanoparticle probes (e.g. SmartFlare™), in situ hybridization (e.g. RNAscope®), microarray, nucleic acid sequencing, and PCR-based assays may be designed as set forth above.

In these exemplary methods or in other methods for nucleic acid detection, aberrant splice variants may be identified using probes, primers, or other reagents which specifically recognize the nucleic acid sequence that is present in the aberrant splice variant but absent in the canonical splice variant. In other embodiments, the aberrant splice variant is identified by detecting the sequence that is specific to the aberrant splice variant in the context of the junction in which it occurs, i.e., the unique sequence is flanked by the sequences which are present on either side of the splice junction in the canonical splice variant. In such cases, the portion of the probe, primer, or other detection reagent that specifically recognizes its target sequence may have a length that corresponds to the length of the aberrant sequence or to or a portion of the aberrant sequence. In other embodiments, the portion of the probe, primer, or other detection reagent that specifically recognizes its target sequence may have a length that corresponds to the length of the aberrant sequence plus the length of a chosen number of nucleotides from one or both of the sequences which flank the aberrant sequence at the splice junction. Generally, the probe or primer should be designed with a sufficient length to reduce non-specific binding. Probes, primers, and other reagents that detect aberrant or canonical splice variants may be designed according to the technical features and formats of a variety of methods for detection of nucleic acids.

SF3B1 Modulators

A variety of SF3B1 modulating compounds are known in the art, and can be used in accordance with the methods described herein. In some embodiments, the SF3B1 modulating compound is a pladienolide or pladienolide analog. A “pladienolid analog” refers to a compound which is structurally related to a member of the family of natural products known as the pladienolides. Plandienolides were first identified in the bacteria Streptomyces platensis (Sakai, Takashi; Sameshima, Tomohiro; Matsufuji, Motoko; Kawamura, Naoto; Dobashi, Kazuyuki; Mizui, Yoshiharu. “Pladienolides, New Substances from Culture of Streptomyces platensis Mer-11107. I. Taxonomy, Fermentation, Isolation and Screening.” The Journal of Antibiotics. 2004, Vol. 57, No. 3). One of these compounds, pladienolide B, targets the SF3B spliceosome to inhibit splicing and alter the pattern of gene expression (Kotake et al., “Splicing factor SF3b as a target of the antitumor natural product pladienolide”, Nature Chemical Biology 3:570-575 [2007]). Certain pladienolide B analogs are described in WO 2002/060890; WO 2004/011459; WO 2004/011661; WO 2004/050890; WO 2005/052152; WO 2006/009276; and WO 2008/126918.

U.S. Pat. Nos. 7,884,128 and 7,816,401, both entitled “Process for Total Synthesis of Pladienolide B and Pladienolide D,” describe methods for synthesizing pladienolide B and D. Synthesis of pladienolide B and D may also be performed using methods described in Kanada et al., “Total Synthesis of the Potent Antitumor Macrolides Pladienolide B and D,” Angew. Chem. Int. Ed. 46:4350-4355 (2007). Kanada et al., U.S. Pat. No. 7,550,503, and International Publication No. WO 2003/099813 (WO '813), entitled “Novel Physiologically Active Substances,” describe methods for synthesizing E7107 (Compound 45 of WO '813) from pladienolide D (11107D of WO '813). In some embodiments, the SF3B1 modulator is pladienolide B. In other embodiments, the SF3B1 modulator is pladienolide D. In further embodiments, the SF3B1 modulator is E7107.

In some embodiments, the SF3B1 modulator is a compound described in U.S. application Ser. No. 14/710,687, filed May 13, 2015, which is incorporated herein by reference in its entirety. In some embodiments, the SF3B1 modulating compound is a compound having one of formulas 1-4 as set forth in Table 2. Table 2. Exemplary SF3B1 modulating compounds.

Compound Structure

1

2

3

4

The methods described herein may be used to evaluate known and novel SF3B1 modulating compounds.

Methods of Treatment

Various embodiments of the invention include treating a patient diagnosed with cancer using an SF3B1 modulator. In certain instances, cancer cells from the patient have been determined to have a mutant SF3B1 protein. Specific SF3B1 mutants include E622D, E622K, E622Q, E622V, Y623C, Y623H, Y623S, R625C, R625G, R625H, R625L, R625P, R625S, N626D, N626H, N626I, N626S, N626Y, H662D, H662L, H662Q, H662R, H662Y, T663I, T663P, K666E, K666M, K666N, K666Q, K666R, K666S, K666T, K700E, V701A, V701F, V701I, I704F, I704N, I704S, I704V, G740E, G740K, G740R, G740V, K741N, K741Q, K741T, G742D, D781E, D781G, or D781N. In certain embodiments, SF3B1 mutants are chosen from K700E, K666N, R625C, G742D, R625H, E622D, H662Q, K666T, K666E, K666R, G740E, Y623C, T663I, K741N, N626Y, T663P, H662R, G740V, D781E, or R625L. In additional embodiments, the cancer cells have been tested to measure the amount of one or more splice variants selected from Table 1. Specific splice variants associated with neomorphic SF3B1 mutations are shown in Table 1 and described in the section on splice variants above.

In certain embodiments, a cancer patient determined to have a mutant SF3B1 protein is treated with an SF3B1 modulator as described in U.S. application Ser. No. 14/710,687, filed May 13, 2015.

EXAMPLES Example 1: SF3B1 Mutations Induce Abnormal Splicing in a Lineage-Specific Manner

To investigate splicing alterations associated with SF3B1 mutations (“SF3B1^(MUT)”) across multiple tumor types, an RNA-Seq quantification and differential splicing pipeline was developed and used to analyze RNA-Seq profiles from the following samples:

-   -   all SF3B1^(MUT) samples in The Cancer Genome Atlas (TCGA; from         81 patients in all, representing 16 cancer types), and 40 wild         type SF3B1 (SF3B1^(WT)) samples from each of the breast         cancer (20) and melanoma (20) cohorts in TCGA,     -   seven SF3B1^(MUT) and seven SF3B1^(WT) CLL patient samples         obtained from the Lymphoma/Myeloma Service in the Division of         Hematology/Oncology at the New York Weill Cornell Medical         Center.

RNA-Seq Quantification Methods

Splice junctions were quantified directly from alignments (BAM files) to facilitate discovery of unannotated splice variants. For internally generated RNA-Seq data, reads were aligned to the human reference genome hg19 (GRCh37) by MapSplice and quantified by RSEM against the TCGA GAF 2.1 isoform and gene definition, emulating the TCGA “RNASeqV2” pipeline (see https://cghub.ucsc.edu/docs/tcga/UNC_mRNAseq_summary.pdf). Splice junction counts generated by MapSplice were used for downstream processing. For TCGA RNA-Seq data, comprehensive splice junction counts generated by MapSplice were not available; instead TCGA “Level 3” splice junction data reports mapped read counts for a predefined set of splice junctions from reference transcriptomes. To reconstruct genome-wide splice junction counts comparable to internally-generated RNA-Seq samples, raw RNA-Seq alignments (BAM files) were obtained from CGHub (https://cghub.ucsc.edu/) and any reads that span across a potential splice junction were directly counted. RSEM-estimated gene expression read counts were gathered directly from the TCGA RNA-SeqV2 Level 3 data matrices.

Because MapSplice only provides exon-exon junction counts, estimates of read counts spanning each intron-exon junction were required for identification of intron-retention splice variants. For every splice junction in each BAM file, reads with at least a 3-bp overhang across each of the 3′ and 5′ intron-exon junctions were counted.

For all manipulation of spliced reads within BAM files, a custom Python module “splicedbam” (available at https://github.com/h3biomed/splicedbam) was used, which uses the “pysam” extension of samtools (Li, H., et al., “The Sequence Alignment/Map format and SAMtools.” Bioinformatics, 2009 Aug. 15; 25(16):2078-9).

In some instances, splice junctions had very low counts, occasionally due to sequencing and alignment errors. Therefore, only splice junctions that had at least a total of 10 counts on average from either SF3B1^(WT) or SF3B1^(1T) cohorts were included in downstream analyses.

Differential Splicing Detection Methods

In order to detect differential usage of a splice variant in one cohort relative to another, independent of gene expression changes and pre-defined alternative splicing models, a computational differential splicing pipeline was developed that converts splice junction counts into percentages of junction usage at splice sites with multiple possible junctions. The percentage of junction usage is a measurement of the occurrence of one splice variant relative to all other splice variants that share the same splice site. For instance, a splice variant with an alternative 3′ splice site must share its 5′ splice site with another splice variant. Therefore, for each shared splice site, the raw counts of each splice variant were divided by the total counts of all splice variants that utilize the shared splice site in order to derive a ratio. This ratio was then multiplied by 100 to convert it to a percentage. For each sample, the sum of all of the percentages of splice variants that share the same splice site will equal 100. The transformation of raw counts of each splice variant into a percentage of all splice variants sharing a splice site is itself a normalization to reduce the effect of gene expression changes. The percentages for canonical and aberrant junctions are listed in Table 1 as “Avg WT %” and “Avg Ab. %,” respectively. Differences between these percentages were assessed for statistical significance by using the moderated t-test defined in the Bioconductor's limma package (available at http://www.bioconductor.org). The statistical p-values were corrected into q values using the Benjamini-Hochberg procedure, and listed as “FDR Q-Values” in Table 1. Any splice variant that satisfied a q value of less than or equal to 0.05 was considered statistically significant.

The conversion of raw junction counts into percentage junction usage can introduce noise in some instances, i.e., when a gene in which a splice variant occurs is expressed in one cohort but has very low expression or is not expressed at all in another cohort. To address this, an additional filtering step was introduced. For each up-regulated splice variant in an SF3B1^(MUT) sample that satisfies the above q value threshold, its corresponding canonical splice variant must be down-regulated in the SF3B1^(MUT) sample and also must also satisfy the q value threshold for the up-regulated splice variant to be considered an aberrant splice variant.

Identification of Aberrant Splice Variants in Neomorphic SF3B1^(MUT) Patient Samples

Initially, this framework was applied to a subset of known SF3B1^(MUT) cancers or wild-type counterparts from The Cancer Genome Atlas (TCGA; luminal A primary breast cancer: 7 SF3B1^(K700E) and 20 SF3B1^(WT); metastatic melanoma: 4 SF3B1^(MUT); and 20 SF3B1^(WT)) and internally generated 7 SF3B1^(MUT) and 7 SF3B1^(WT) CLL patient samples. This analysis revealed 626 aberrant splice junctions to be significantly upregulated in SF3B1^(MUT) compared to SF3B1^(WT). The vast majority of aberrant splicing events use an alternative 3′ss (see Table 1, “Event” column).

The computational screening of aberrant splicing events revealed a pattern of tumor-specific splicing events in breast cancer, melanoma and CLL in neomorphic SF3B1^(MUT) samples (Table 1). In addition, a set of tumor-non-specific events (i.e., splicing events found in at least two tumor types) was observed. Some splice variants of genes with tumor-specific splicing events occur in genes with higher mRNA expression, indicating that some of the observed tumor-specific splicing results from gene expression differences (FIG. 2).

To characterize the effect of aberrant splicing in all SF3B1 variants across cancer types, RNA-Seq data for the remaining 70 SF3B1^(MUT) patients from 14 cancer types in TCGA were quantified, and an unsupervised clustering analysis was done using all 136 samples. This clustering separated splicing events associated with neomorphic SF3B1 mutants from those associated with wild-type SF3B1 or non-neomorphic SF3B1 mutants. For example, splicing patterns associated with neomorphic SF3B1 mutants were observed in breast cancer (SF3B1^(K666E), SF3B1^(N626D)), lung adenocarcinoma (SF3B1^(K741N), SF3B1^(G740V)), and bladder cancer (SF3B1^(R625C)) patient samples, as splicing events in these samples clustered with those in SF3B1^(K700E) neomorphic samples, whereas the splicing profiles for other SF3B1 mutant samples were similar to those of SF3B1^(WT) samples of the same tumor type. A listing of SF3B1 mutants whose splicing profiles clustered with those of neomorphic SF3B1 mutants is provided in Table 3, column 1. Additional SF3B1 mutations that are predicted to be neomorphic are listed in Table 3, column 2. A schematic diagram showing the locations of all mutations provided in Table 3 is shown in FIG. 3.

TABLE 3 Select SF3B1 mutations SF3B1 Mutations with Splicing Profiles Clustering with Neomorphic Predicted Neomorphic SF3B1 Mutations SF3B1 Mutations K700E K666Q K666N K666M R625C H662D G742D D781G R625H I704F E622D I704N H662Q V701F K666T R625P K666E R625G K666R N626D G740E H662Y Y623C N626S T663I G740R K741N N626I N626Y N626H T663P V701I H662R R625S G740V K741T D781E K741Q R625L I704V I704S E622V Y623S Y623H V701A K666S H662L G740K E622Q E622K D781N

Example 2: Validation of Aberrant Splice Variants in Cell Lines

Aberrant splicing in cell line models was analyzed by collecting RNA-Seq profiles for a panel of cell lines with endogenous SF3B1 neomorphic mutations (pancreatic adenocarcinoma Panc 05.04: SF3B1^(Q699H/K700E) double mutant; metastatic melanoma Colo829: SF3B1^(P718L); and lung cancer NCI-H358: SF3B1^(A745V); obtained from the American Type Culture Collection [ATCC] or RIKEN BioResource Center and cultured as instructed) and from several SF3B1^(WT) cell lines from either the same tumor types (pancreatic adenocarcinoma Panc 10.05, HPAF-II, MIAPaCa-2, Panc04.03, PK-59, lung cancer NCI-H358, NCI-H1792, NCI-H1650, NCI-H1975, NCI H1838) or normal control cells of the same patient (Epstein-Barr virus [EBV]-transformed B lymphoblast colo829BL). RNA-Seq profiles were also collected from isogenic pre B-cell lines (Nalm-6) engineered via AAV-mediated homology to express SF3B1^(K700E) (Nalm-6 SF3B1^(K700E)) or a synonymous mutation (Nalm-6 SF3B1^(K700K)). The isogenic cell lines Nalm-6 SF3B1^(K700E) and Nalm-6 SF3B1^(K700K) generated at Horizon Discovery, were cultured in presence of Geneticin (0.7 mg/ml, Life Technologies) for selection. All RNA-Seq analysis was performed using the same pipeline described for patient samples in Example 1. Unsupervised clustering of cell lines using the aberrant splice junctions identified in patients resulted in clear segregation of Panc 05.04 and Nalm-6 SF3B1^(K700E) from wild-type and other SF3B1-mutant cells.

A NanoString® assay was developed to quantify aberrant and canonical splice variants and was validated using the same cell panel. For the NanoString® assay, 750 ng of purified total RNA was used as template for the nCounter® (NanoString Technologies®) expression assay using a custom panel of NanoString® probes. The sample preparation was set up as recommended (NanoString® Technologies protocol no. C-0003-02) for an overnight hybridization at 65° C. The following day, samples were processed through the automated nCounter® Analysis System Prep Station using the high sensitivity protocol (NanoString® Technologies protocol no. MAN-00029-05) followed by processing through the nCounter® Analysis System Digital Analyzer (protocol no. MAN-00021-01) using 1150 FOVs for detection. Data was downloaded and analyzed for quality control metrics and normalization using the nSolver™ Analysis Software (NanoString Technologies®). The data was first normalized for lane-to-lane variation using the positive assay controls provided by the manufacturer (NanoString® positive controls A-F [containing in vitro transcribed RNA transcripts at concentrations of 128 fM, 32 fM, 8 fM, 2 fM, 0.5 fM, and 0.125 fM, each pre-mixed with NanoString® Reporter CodeSet probes])). Any samples with normalization factors <0.3 and >3 were not considered for further analysis. This was followed by content normalization using the geo-mean of GAPDH, EEF1A1 and RPLP0. All samples were within the recommended 0.1-10 normalization factor range. Each normalized value was then checked to ensure that it was at least two standard deviations higher than the average of background signal recorded for that lane. Any value below that was considered below detection limit. These normalized values were taken for further bioinformatics and statistical analysis.

As observed in the RNA-Seq analysis, only the Panc 05.04 and isogenic Nalm-6 SF3B1^(K700E) cell lines showed clear presence of aberrant splicing (FIG. 4).

Analysis of SF3B1 Mutant SF3B1Q^(699H)

The Panc 05.04 cell line carries the neomorphic mutation SF3B1^(K700E) and an additional mutation at position 699 (SF3B1^(Q699H)). To evaluate the functional relevance of this second mutation, SF3B1^(Q699H) and SF3B1^(K700E) mutant SF3B1 proteins were expressed alone or in combination in 293FT cells (FIG. 5) for analysis of RNA by NanoString®. To express the mutants in 293FT cells, mammalian expression plasmids were generated using the Gateway technology (Life Technologies). First, the HA-tag mxSF3B1 wild-type (Yokoi, A. et al. “Biological validation that SF3b is a target of the antitumor macrolide pladienolide.” FEBS J. 278:4870-4880 [2011]) was cloned by PCR into the pDONR221, then the mutations were introduced using the site-directed mutagenesis kit (QuikChange II XL, Agilent). LR reaction was performed to clone all the HA-tag mxSF3B1 wild-type and mutants into the pcDNA-DEST40 (Life Technologies). 293FT cells (Life Technologies), cultured according to the manufacturer's instructions, were seeded on 6 wells/plate and transfected with generated plasmid using Fugene (Roche). One μg of DNA per pcDNA-DEST40 HA-mxSF3B1 construct was used for each transient transfection, generated in triplicates. Forty-eight hours after transfection, cells were collected to isolate protein and RNA for western blot and NanoString® analysis, respectively. Protein extracts were prepared by lysing the cells with RIPA (Boston BioProducts). Twenty-three μg of protein was loaded in a SDS-PAGE gel and identified using SF3B1 antibody (a-SAP 155, MBL) and anti-GAPDH (Sigma). Li-Cor donkey-anti-mouse 800CW and Li-Cor donkey-anti-rabbit 800CW were used as secondary antibodies and detected by Odyssey imager (Li-Cor). RNA was isolated from the cells and retrotranscribed using MagMax for Microarray and Superscript VILO II (Life Technologies), respectively, according to the manufacturer manual, and then analyzed with the NanoString® assay.

Expression of SF3B1^(K700E) and SF3B1^(Q699H/K700E) induced aberrant splicing, whereas SF3B1^(Q699H) alone or SF3B1^(A745V) or SF3B1^(R1074H) (a substitution conferring resistance to the spliceosome inhibitor pladienolide B) did not induce aberrant splicing (FIG. 6), indicating that SF3B1Q^(999H) is a non-functional substitution.

These data confirm that Panc 05.04 and Nalm-6 SF3B1^(K700E) isogenic cells are representative models to study the functional activity of SF3B1 neomorphic mutations and the activity of splicing inhibitors in vitro and in vivo.

Example 3: Neomorphic SF3B1 Mutations Induce Abnormal mRNA Splicing

The functional activity of neomorphic mutations found in SF3B1^(MUT) cancers was analyzed by expressing SF3B1^(WT), neomorphic SF3B1 mutants, or SF3B1^(K700R) (the mutation observed in a renal clear cell carcinoma patient that clusters with SF3B1^(WT) patients) in 293FT cells and determining splicing aberrations by NanoString®. The expression of all constructs was confirmed by western blot (FIG. 7). All SF3B1 neomorphic mutations tested demonstrated the same usage of alternative splice sites observed in patient samples (“MUT isoform” in FIG. 8), but SF3B1^(K700R) and SF3B1^(WT) did not show aberrant splicing (FIG. 8). Moreover, the expression of none of the SF3B1 constructs changed the overall gene expression (“PAN-gene” in FIG. 8) or the canonical splice isoforms (“WT isoform” in FIG. 8). This indicated both a correlation between the presence of the neomorphic SF3B1 mutations and alternative splicing as well as similar functional activity of the different neomorphic mutations, as was indicated by the RNA-Seq analysis of patient samples.

The correlation between the SF3B1^(K700E) neomorphic mutation and aberrant splicing was analyzed using tetracycline-inducible shRNA to selectively knockdown the neomorphic SF3B1 mutant or SF3B1^(WT) allele in Panc 05.04 and Panc 10.05 cell lines (neomorphic SF3B1^(MUT) and SF3B1^(WT) cell lines, respectively; obtained from the American Type Culture Collection [ATCC] or from RIKEN BioResource Center and cultured as instructed).

For the knockdown experiment, virus encoding shRNA was prepared in LentiX-293T cells (Clontech), which were cultured according to the manufacturer's instruction. The inducible shRNA were cloned into AgeI and EcoRI of the pLKO-iKD-H1 euro vector. The sequences of hairpins were:

shRNA #13 SF3B1^(PAN) (SEQ ID NO: 1180) GCGAGACACACTGGTATTAAG, shRNA #8 SF3B1^(WT) (SEQ ID NO: 1181) TGTGGATGAGCAGCAGAAAGT; and shRNA #96 SF3B1^(MUT) (SEQ ID NO: 1182) GATGAGCAGCATGAAGTTCGG.

Cells were transfected with 2.4 μg of target pLKO-shRNA plasmid, plus 2.4 μg of p Δ 8.91 (packaging), and 0.6 μg VSVG (envelope) using TransIT reagent (Mirus). The virus was used to infect Panc 05.04 and Panc 10.05 by spin infection using Polybrene (Millipore). The day after infection, the cells were cultured in selecting media (1.25 μg/ml Puromycin [Life Technologies]) for 7 days to select for shRNA-expressing cells. The selected cells were cultured in the presence or absence of Doxycycline hyclate (100 ng/mL; Sigma) to induce the shRNA. Cells were harvested for protein and RNA at day 4 post-induction. In addition, cells were seeded for colony forming assay and CellTiter-Glo® assay (Promega). At day 9, cells were fixed with formaldehyde and stained with crystal violet.

To confirm SF3B1 knockdown using western blots, protein extracts were prepared by lysing the cells with RIPA (Boston BioProducts). Twenty to 25 μg of protein from each sample was separated by SDS-PAGE and transferred to nitrocellulose membranes (iblot, Life Technologies). Membranes were first blocked with Odyssey Blocking Buffer (Li-Cor) and then incubated with SF3B1 antibody (a-SAP 155, MBL) and anti-GAPDH (Sigma). Li-Cor donkey-anti-mouse 800CW and Li-Cor donkey-anti-rabbit 800CW were used as secondary antibodies and detected by Odyssey imager (Li-Cor).

To confirm SF3B1 knockdown by allele specific qPCR, RNA was isolated from the cells and retrotranscribed using MagMax for Microarray and Superscript VILO II (Life Technologies), respectively according to the manufacturer manual. qPCR was performed using ViiA7 (Life Technologies). The reaction included 20-50 ng cDNA, Power SYBR green master mix (Life Technologies) and 300 nM primers. The following primers were used:

SF3B1^(WT): (SEQ ID NO: 1183) FW 5′-GACTTCCTTCTTTATTGCCCTTC and (SEQ ID NO: 1184) RW 5′-AGCACTGATGGTCCGAACTTTC, SF3B1^(MUT): (SEQ ID NO: 1185) FW 5′-GTGTGCAAAAGCAAGAAGTCC and (SEQ ID NO: 1186) RW 5′-GCACTGATGGTCCGAACTTCA, SF3B1^(PAN): (SEQ ID NO: 1187) FW 5′-GCTTGGCGGTGGGAAAGAGAAATTG and (SEQ ID NO: 1188) RW 5′-AACCAGTCATACCACCCAAAGGTGTTG, β-actin (internal control): (SEQ ID NO: 1189) FW 5′-GGCACCCAGCACAATGAAGATCAAG and (SEQ ID NO: 1190) RW 5′-ACTCGTCATACTCCTGCTTGCTGATC. Biological and technical triplicates were performed.

The western blotting and allele specific PCR both confirmed knockdown of the SF3B1 alleles (FIGS. 9 and 10).

To determine the association between the expression of SF3B1 mutations and aberrant splicing, RNA isolated from the cells following doxycycline-induced knockdown was analyzed by NanoString®. In Panc 05.04, after knockdown of the neomorphic SF3B1^(MUT) allele, the aberrant splice variants were downregulated and the canonical splice variants were upregulated, whereas the opposite was observed with selective depletion of the SF3B1^(WT) allele (FIG. 11A), indicating that the neomorphic SF3B1^(MUT) protein does not possess wild-type splicing activity. The expression of a pan shRNA induced the regulation of all splice variants as well as the depletion of SF3B1^(WT) in Panc 10.05 cells (FIG. 11B). SF3B1^(PAN) knockdown impaired growth and colony formation in both cell lines, while a minimal effect was observed with selective depletion of neomorphic SF3B1^(MUT) in Panc05.04 cells (FIGS. 12 and 13). When the SF3B1^(WT) allele was knocked down in Panc 05.04 cells, only a partial viability effect was observed, whereas SF3B1^(PAN) knockdown prevented colony formation and cell proliferation (FIGS. 12 and 14), indicating that pan-inhibition of SF3B1 leads to antitumor activity in vitro and in vivo.

Example 4: Modulation of Neomorphic SF3B1^(MUT) Splicing

Overall Effect of E7107 on Splicing

E7107 is a small-molecule compound that inhibits splicing by targeting the U2 snRNP-associated complex SF3B (Kotake, Y. et al. “Splicing factor SF3b as a target of the antitumor natural product pladienolide.” Nat Chem Biol 3, 570-575, doi:10.1038/nchembio.2007.16 [2007]). The ability of E7107 to inhibit splicing was observed in an in vitro splicing assay (IVS) using the substrate Ad2 (Pellizzoni, L., Kataoka, N., Charroux, B. & Dreyfuss, G. “A novel function for SMN, the spinal muscular atrophy disease gene product, in pre-mRNA splicing.” Cell 95, 615-624 [1998]) and nuclear extracts from the Nalm-6 isogenic cell lines or 293F cells (Life Technologies; cultured according to the manufacturer's instructions) expressing Flag-tag SF3B1^(WT) or SF3B1^(K700E), as follows.

Nuclear extracts were prepared from 293F cells transfected with pFLAG-CMV-2-SF3B1 plasmids, or from isogenic Nalm-6 cells (SBH Sciences). The plasmids were generated by cloning the mxSF3B1 gene into the HindIII and KpnI sites of pFLAG-CMV2 (Sigma), and the mutations mxSF3B1^(K700E), mxSF3B1^(R1074H) and mxSF3B1^(K700E-R1074H) were introduced using the same site-directed mutagenesis kit. Cell pellets were resuspended in hypotonic buffer (10 mM HEPES pH 7.9, 1.5 mM MgCl₂, 10 mM KCl, 0.2 mM PMSF, and 0.5 mM DTT; for Nalm-6 cells, 40 mM KCl was used). The suspension was brought up to a total of five packed cell volumes (PCV). After centrifugation, the supernatant was discarded, and the cells were brought up to 3 PCV with hypotonic buffer, and incubated on ice for 10 minutes. Cells were lysed using a dounce homogenizer and then centrifuged. The supernatant was discarded, and the pellet was resuspended with ½ packed nuclear volume (PNV) of low salt buffer (20 mM HEPES pH 7.9, 1.5 mM MgCl₂, 20 mM KCl, 0.2 mM EDTA, 25% glycerol, 0.2 mM PMSF, 0.5 mM DTT), followed by ½ PNV of high salt buffer (same as low salt buffer except 1.4M KCl was used). The nuclei were gently mixed for 30 minutes before centrifuging. The supernatant (nuclear extract) was then dialyzed into storage buffer (20 mM HEPES pH 7.9, 100 mM KCl, 0.2 mM EDTA, 20% glycerol, 0.2 mM PMSF, 0.5 mM DTT). Protein concentration was determined using NanoDrop 8000 UV-Vis spectrophotometer (Thermo Scientific).

For in vitro splicing (IVS) reactions, an Ad2-derived sequence (Pellizzoni, L., Kataoka, N., Charroux, B. & Dreyfuss, G. “A novel function for SMN, the spinal muscular atrophy disease gene product, in pre-mRNA splicing.” Cell 95, 615-624 [1998]) was cloned into the pGEM-3Z vector (Promega) using EcoRI and XbaI restriction sites. The resulting pGEM-3Z-Ad2 plasmid was linearized using XbaI, purified, resuspended in TE buffer, and used as a DNA template in the in vitro transcription reaction. The Ad2 pre-mRNA was generated and purified using MEGAScript T7 and MegaClear kits, respectively (Invitrogen). Twenty μL splicing reactions were prepared using 80 μg nuclear extracts, 20U RNAsin Ribonuclease inhibitor (Promega), 10 ng Ad2 pre-mRNA, and varying concentrations of E7107. After a 15 minute pre-incubation, activation buffer (0.5 mM ATP, 20 mM creatine phosphate, 1.6 mM MgCl₂) was added to initiate splicing, and the reactions were incubated for 90 minutes. RNA was extracted using a modified protocol from a RNeasy 96 Kit (Qiagen). The splicing reactions were quenched in 350 μL Buffer RLT Plus (Qiagen), and 1.5 volume ethanol was added. The mixture was transferred to an RNeasy 96 plate, and the samples were processed as described in the kit protocol. RNA was diluted 1/10 with dH₂O. 10 μL RT-qPCR reactions were prepared using TaqMan RNA-to-C_(T) 1-step kit (Life Technologies), 8.5 μL RNA, and 1 μL of Ad2 mRNA primers/probe set (FW 5′ ACTCTCTTCCGCATCGCTGT (SEQ ID NO: 1191), RW 5′-CCGACGGGTTTCCGATCCAA (SEQ ID NO: 1192) and probe 5′ CTGTTGGGCTCGCGGTTG (SEQ ID NO: 1193)).

To evaluate pSF3B1, in vitro splicing reactions were prepared as described above. To quench the reactions, 6× Laemmli Buffer (Boston Bioproducts) was added, and the samples were subjected to SDS-PAGE gels (Life Technologies). The separated proteins were transferred onto nitrocellulose membranes then blocked with blocking buffer (50% Odyssey Blocking Buffer (Li-Cor Biosciences) and 50% TBST). The blots were incubated with anti-SF3B1 antibody overnight, after several washes in TBST, they were incubated with IRDye 680LT donkey-α-mouse-IgG antibody and visualized using an Odyssey CLx imaging system (Li-Cor Biosciences).

E7107 was able to inhibit splicing in nuclear extracts from both the Nalm-6 cells or the 293F cells expressing Flag-tag SF3B1^(WT) or SF3B1^(K700E) (FIGS. 15A and 15B).

E7107 Binds Both SF3B1^(WT) and SF3B1^(K700E) Proteins

The ability of E7107 to bind both SF3B1^(WT) and SF3B1^(K700E) proteins was evaluated in a competitive binding assay using Flag-tag SF3B1 proteins immunoprecipitated with anti-Flag antibody from transiently transfected 293F cells. Batch immobilization of antibody to beads was prepared by incubating 80 μg of anti-SF3B1 antibody (MBL International) and 24 mg anti-mouse PVT SPA scintillation beads (PerkinElmer) for 30 minutes. After centrifugation, the antibody-bead mixture was resuspended in PBS supplemented with PhosSTOP phosphatase inhibitor cocktail (Roche) and complete ULTRA protease inhibitor cocktail (Roche). Nuclear extracts were prepared by diluting 40 mg into a total volume of 16 mL PBS with phosphatase and protease inhibitors, and the mixture was centrifuged. The supernatant was transferred into a clean tube, and the antibody-bead mixture was added and incubated for two hours. The beads were collected by centrifuging, washed twice with PBS+0.1% Triton X-100, and resuspended with 4.8 mL of PBS. 100 μL binding reactions were prepared using slurry and varying concentrations of E7107. After 15 minutes pre-incubation at room temperature, one nM ³H-probe molecule (described in Kotake, Y. et al. Splicing factor SF3b as a target of the antitumor natural product pladienolide. Nat Chem Biol 3, 570-575, doi:10.1038/nchembio.2007.16 [2007]) was added. The mixture was incubated at room temperature for 15 minutes, and luminescence signals were read using a MicroBeta2 Plate Counter (PerkinElmer).

As shown in FIG. 16A, E7107 was able to competitively inhibit binding of the ³H-probe molecule in a similar manner to either SF3B1^(WT) (IC₅₀: 13 nM) or SF3B1^(K700E) (IC₅₀: 11 nM).

Effect of E7107 and Other Compounds on Normal and Aberrant Splicing

E7107 was also tested in vitro in Nalm-6 isogenic cell lines for the ability to modulate normal and aberrant splicing induced by SF3B1^(WT) and SF3B1^(K700E) protein. Nalm-6 isogenic cells were treated with increasing concentrations of E7107 for six hours and RNA was analyzed by qPCR. As shown in FIG. 16B, canonical splicing was observed, with accumulation of pre-mRNA for EIF4A1 and downregulation of the mature mRNA SLC25A19 observed in both cell lines. Additionally, downregulation of mature mRNA of the two abnormally spliced isoforms of COASY and ZDHHC16 was observed in Nalm-6 SF3B1^(K700E) (FIG. 16B).

To investigate the broader activity of E7107 on normal and aberrant splicing, RNA from Nalm-6 isogenic cells treated for two and six hours at 15 nM was analyzed by NanoString®. Only partial inhibition of splicing was observed at two hours in both isogenic cell lines, and at the level of gene, WT-associated isoforms, and MUT-associated isoform expression. After six hours of treatment, clear inhibition was detected for all isoforms quantified (FIG. 17). Similar results were obtained by RNA-Seq analysis of isogenic cell lines treated for six hours with E7107 at 15 nM (FIG. 18). Normal and aberrant splicing in the isogenic cell lines was also analyzed by RNA-Seq following treatment with one of additional compounds having formulas 1 or 2. Like E7107, each of these additional compounds inhibited expression of both WT-associated and MUT-associated RNA isoforms (FIG. 19; compound is indicated by formula number above each vertical pair of graphs). For the RNA-Seq analysis, cells were washed with PBS after treatment with E7107 or other test compound, and RNA was isolated using PureLink (Life Technology) as reported in the manufacturer's manual. cDNA library preparation, sequencing and raw read filtering was performed as described in Ren, S. et al. “RNA-Seq analysis of prostate cancer in the Chinese population identifies recurrent gene fusions, cancer-associated long noncoding RNAs and aberrant alternative splicings.” Cell Res 22, 806-821, doi:10.1038/cr.2012.30 (2012).

In addition, the ability of E7107 to modulate splicing was tested in mice bearing human tumor xenografts. Nalm-6 isogenic xenograft mice were generated by subcutaneously implanting 10×10⁶ Nalm-6 isogenic cells into the flank of CB17-SCID mice, and tumors from these mice were collected at different timepoints after a single intravenous (IV) dose of E7107 (5 mg/kg) and analyzed to determine compound concentrations and splicing regulation. RNA was isolated from the tumors using RiboPure™ RNA purification kit (Ambion®) and used for NanoString® assay or qPCR. The RNA was retrotranscribed according to the instructions of the SuperScript® VILO™ cDNA synthesis kit (Invitrogen™) and 0.04 μl of cDNA was used for qPCR. qPCR for pre-mRNA EIF4A1 and mature mRNA SLC24A19 and pharmacokinetic evaluation were performed as described in Eskens, F. A. et al. “Phase I pharmacokinetic and pharmacodynamic study of the first-in-class spliceosome inhibitor E7107 in patients with advanced solid tumors.” Clin Cancer Res 19, 6296-6304, doi:10.1158/1078-0432.CCR-13-0485 (2013). The primers and probes used for ZDHHC16 were the following: FW 5′-TCTTGTCTACCTCTGGTTCCT (SEQ ID NO: 1194), RW 5′ CCTTCTTGTTGATGTGCCTTTC (SEQ ID NO: 1195) and probe 5′ FAM CAGTCTTCGCCCCTCTTTTCTTAG (SEQ ID NO: 1196). The primers and probes used for COASY were the following: FW 5′-CGGTGGTGCAAGTGGAA (SEQ ID NO: 1197), RW 5′-GCCTTGGTGTCCTCATTTCT (SEQ ID NO: 1198) and probe 5′-FAM-CTTGAGGTTTCATTTCCCCCTCCC (SEQ ID NO: 1199). E7107 reached similar drug concentrations and modulated canonical splicing (accumulation of pre-mRNA for EIF4A1 and downregulation of the mature mRNA SLC25A19) in both Nalm-6 SF3B1^(K700K) and Nalm-6 SF3B1^(K700E) models and downregulated abnormal splicing of COASY and ZDHHC16 in the Nalm-6 SF3B1^(K700E) cells (FIG. 20), as observed in vitro. The canonical and aberrant splice mRNA isoforms were downregulated by E7107 as early as one hour following administration of the compound, and expression normalized shortly after treatment (FIG. 21), consistent with E7107 pharmacokinetic profile. Similar results were observed in a Panc 05.04 neomorphic SF3B1 xenograft model (FIG. 22). All these data indicate that E7107 is a pan-splicing modulator that can bind and inhibit SF3B1^(WT) and SF3B1^(K700E) proteins in vitro and in vivo.

Example 5: E7107 has Anti-Tumor Activity Via SF3B1 Modulation

SF3B1 modulator E7107 was tested for antitumor activity in vivo by determining the effect of E7107 in a subcutaneous model of Nalm-6 SF3B1^(K700E). 10×10⁶ Nalm-6 SF3B1^(K700E) were subcutaneously implanted into the flank of CB17-SCID mice, and mice were administered E7107 intravenously once a day for 5 consecutive days (QD×5) at three well tolerated dose levels (1.25, 2.5 and 5 mg/kg). After this dosing, the animals were monitored until they reached either of the following endpoints: 1) excessive tumor volume measured three times a week (tumor volume calculated by using the ellipsoid formula: (length×width)/2), or 2) development of any health problem such as paralysis or excessive body weight loss. Partial regression (PR) and complete regression (CR) are defined as 3 consecutive tumor measurements <50% and <30% of starting volume respectively.

In the 1.25 mg/kg group, all animals (n=10) reached complete regression (CR) in the Nalm-6 SF3B1^(K700E) xenograft group. In the 2.5 mg/kg group, 10/10 CRs were observed in the Nalm-6 SF3B1^(K700E) group by day 9. In the 5 mg/kg group all Nalm-6 SF3B1^(K700E) xenograft animals reached CR as early as 9 days post treatment and had mean survival times of over 250 days (FIGS. 23 and 24). These data demonstrate antitumor activity of SF3B1 modulator in SF3B1^(K700E) xenografts in vivo.

The ability of E7107 to inhibit splicing in CLL patient samples in vitro was determined by isolating RNA from samples of E7107-treated patient cells treated for 6 hours with E7107 at 10 nM and performing RNA-Seq analysis. To do so, cells were washed with PBS after treatment with E7107, and RNA was isolated using PureLink (Life Technology) as reported in the manufacturer's manual. cDNA library preparation, sequencing and raw read filtering was performed as described in Ren, S. et al. “RNA-Seq analysis of prostate cancer in the Chinese population identifies recurrent gene fusions, cancer-associated long noncoding RNAs and aberrant alternative splicings.” Cell Res 22, 806-821, doi:10.1038/cr.2012.30 (2012). As shown in FIG. 25, E7107 inhibited the expression of canonical splice isoforms in SF3B1^(WT) and neomorphic SF3B1^(MUT) patient samples. E7107 was able to modulate aberrant splicing in all CLL patient samples carrying neomorphic SF3B1 mutations.

Other embodiments of the invention will be apparent to those skilled in the art from consideration of the specification and practice of the invention disclosed herein. It is intended that the specification and examples be considered as exemplary only, with a true scope and spirit of the invention being indicated by the following claims. 

1. A method of detecting one or more splice variants selected from rows 1-790 of Table 1 in a biological sample, comprising a) providing a biological sample suspected of containing one or more splice variants; b) contacting the biological sample with one or more nucleic acid probes capable of specifically hybridizing to the one or more splice variants, and c) detecting the binding of the one or more probes to the one or more splice variants.
 2. The method of claim 1, wherein the one or more nucleic acid probes each comprise a label.
 3. The method of claim 1, further comprising contacting the biological sample with one or more additional nucleic acid probes, wherein the additional probes are each labeled with a molecular barcode.
 4. A method of modulating the activity of a neomorphic mutant SF3B1 protein in a target cell, comprising applying an SF3B1-modulating compound to the target cell, wherein the target cell has been determined to express one or more aberrant splice variants selected from rows 1-790 of Table 1 at a level that is increased or decreased relative to the level in a cell not having the neomorphic mutant SF3B1 protein.
 5. A method for evaluating the ability of a compound to modulate the activity of a neomorphic mutant SF3B1 protein in a target cell, comprising the steps of: a) providing a target cell having a mutant SF3B1 protein; b) applying the compound to the target cell; and c) measuring the expression level of one or more splice variants selected from row 1-790 of Table
 1. 6. The method of claim 5, further comprising the step of measuring the expression level of one or more splice variants selected from row 1-790 of Table 1 before step (b).
 7. The method of any one of claims 4-6, wherein the neomorphic mutant SF3B1 protein is selected from E622D, E622K, E622Q, E622V, Y623C, Y623H, Y623S, R625C, R625G, R625H, R625L, R625P, R625S, N626D, N626H, N626I, N626S, N626Y, H662D, H662L, H662Q, H662R, H662Y, T663I, T663P, K666E, K666M, K666N, K666Q, K666R, K666S, K666T, K700E, V701A, V701F, V701I, I704F, I704N, 17045, 1704V, G740E, G740K, G740R, G740V, K741N, K741Q, K741T, G742D, D781E, D781G, or D781N.
 8. The method of any one of claims 5-7, wherein the step of measuring the expression level of one or more splice variants comprises using a nucleic acid quantification assay selected from nucleic acid barcoding, RT-PCR, microarray, nucleic acid sequencing, nanoparticle probes, and in situ hybridization.
 9. The method of any one of claims 5-8, wherein the step of measuring the expression level of one or more splice variants comprises measuring the number of copies of the one or more splice variant RNAs in the target cell.
 10. The method of any one of claims 4-9, wherein the compound is selected from a small molecule, an antibody, an antisense molecule, an aptamer, an RNA molecule, and a peptide.
 11. The method of claim 10, wherein the compound is a small molecule selected from a pladienolide or a pladienolide analog.
 12. The method of claim 11, wherein the pladienolide analog is selected from pladienolide B, pladienolide D, E7107, a compound of formula 1:

a compound of formula 2:

a compound of formula 3:

or a compound of formula 4:


13. The method of any one of claims 4-12, wherein the target cell is obtained from a patient suspected of having myelodysplastic syndrome, chronic lymphocytic leukemia, chronic myelomonocytic leukemia, or acute myeloid leukemia.
 14. The method of any one of claims 4-13, wherein the target cell is obtained from a sample selected from blood or a blood fraction or is a cultured cell derived from a cell obtained from a sample chosen from blood or a blood fraction.
 15. The method of claim 14, wherein the target cell is a lymphocyte.
 16. The method of any one of claims 4-12, wherein the target cell is obtained from a solid tumor.
 17. The method of claim 16, wherein the target cell is a breast tissue cell, pancreatic cell, lung cell, or skin cell.
 18. A method for treating a patient with a neoplastic disorder, comprising administering a therapeutically effective amount of an SF3B1-modulating compound to the patient, wherein a cell from the patient has been determined to: a) contain a neomorphic mutant SF3B1 protein; and b) express one or more aberrant splice variants selected from rows 1-790 of Table 1 at a level that is increased or decreased relative to the level in a cell not having the neomorphic mutant SF3B1 protein.
 19. The method of any one of claims 1-18, wherein one or more of the splice variants is an aberrant variant selected from rows 1, 7, 9, 10, 13, 15, 16, 18, 21, 24, 27, 28, 30, 31, 33, 34, 48, 51, 62, 65, 66, 71, 72, 81, 84, 89, 91, 105, 107, 121, 135, 136, 152, 178, 235, 240, 247, 265, 267, 272, 276, 279, 282, 283, 286, 292, 295, 296, 298, 302, 306, 329, 330, 331, 343, 350, 355, 356, 360, 364, 372, 378, 390, 391, 423, 424, 425, 426, 431, 433, 438, 439, 443, 445, 447, 448, 451, 452, 458, 459, 460, 462, 468, 469, 472, 500, 508, 517, 519, 521, 524, 525, 527, 528, 530, 533, 536, 540, 543, 548, 545, 554, 556, 559, 571, 573, 580, 582, 583, 597, 601, 615, 617, 618, 639, 640, 654, 657, 666, 670, 680, 727, 730, 750, 758, 767, or 774 of Table
 1. 20. The method of any one of claims 1-19, wherein one or more of the splice variants is an aberrant variant selected from rows 21, 31, 51, 81, 118, 279, 372, 401, 426, 443, 528, 543, 545, 548 or 566 of Table
 1. 